Tag Archives: Drugs and Pharmaceuticals

iCell Gene Therapeutics Announces CAR-T Oral and Poster Presentations at 61st American Society of Hematology Annual Meeting

STONY BROOK, N.Y. /ScoopCloud/ -- iCell Gene Therapeutics, a clinical stage biopharmaceutical company focused on immunotherapies for hematologic malignancies, solid tumors, organ rejections and autoimmune disorders, announced today that it will give oral and poster presentations related to its BCMA-CD19 cCAR and CD4-specific CAR programs at the 61st American Society of Hematology (ASH) Annual Meeting to be held December 7-10, 2019 in Orlando, Florida.

ASH abstracts are now available at https://www.hematology.org/.

Oral Presentation:

Title: First-in-Human Trial of BCMA-CD19 Compound CAR with Remarkable Donor-Specific Antibody Reduction
Session: 721. Abstract Number: 38
Saturday, December 7, 2019: 7:45 a.m.
Valencia BC (W415BC), Level 4 (Orange County Convention Center)
Clinicaltrials.govID: NCT04162353

Poster Presentation:

Title: First-in-Human CD4 CAR Clinical Trial on Peripheral T-Cell Lymphoma
Session: 626. Abstract Number: 2881
Sunday, December 8, 2019, 6 p.m. to 8 p.m.
Hall B, Level 2 (Orange County Convention Center)
Clinicaltrials.govID: NCT04162340

About BCMA-CD19 cCAR therapy

BCMA-CD19 cCAR is a compound Chimeric Antigen Receptor (cCAR) immunotherapy with two distinct functional CAR molecules expressing on a T-cell, directed against the surface proteins BCMA and CD19. The diseases treated by BCMA-CD19 cCAR could include autoimmune disorders, and organ rejection. BCMA is expressed in plasma cells, while CD19 is related to B-cells. BCMA-CD19 cCAR is designed to completely remove antibody-producing "roots", plasma cells and B cells, and then re-set the immune system for treating antibody-mediated autoimmune disorders or organ rejections.

BCMA-CD19 cCAR is also aimed to treat multiple myeloma, a challenging disease due to the heterogeneity of myeloma cells, which renders single-antigen targeting CAR T-cell therapy ineffective. BCMA-CD19 cCAR is proposed to target both bulky myeloma cells expressing BCMA, and myeloma stem cells expressing CD19 to effectively eradicate the disease.

About CD4-specific CAR (CD4 CAR) therapy

CD4-specific CAR with a safety switch is designed to treat peripheral T cell lymphoma as CD4 is uniformly expressed on most mature T cell lymphoma, and transient depletion of CD4 is expected. The diseases treated by CD4 CAR could include peripheral T-cell lymphoma (NOS), Sezary syndrome/cutaneous T-cell lymphoma, angioimmunoblastic T-cell lymphoma, adult T cell lymphoma, T-cell prolymphocytic leukemia, T-cell acute lymphoblastic leukemia/lymphoma and T-cell large granular lymphocytic leukemia. Most of these diseases are difficult to treat, with dismal prognoses. An IND has been approved for iCell Gene Therapeutics to initiate a multi-site clinical trial at Stony Brook University Hospital and University of Louisville.

About iCell Gene Therapeutics

iCell Gene Therapeutics, located in Stony Brook, New York, is a clinical-stage biopharmaceutical company developing first-in-class chimeric antigen receptor engineered cells. Clinical studies on our CARvac, T-cell targeted CARs, Compound CARs, Non-gene edited universal CARs and C-TPS1 (depletion of TREG, blockage of PD-L1 pathways and stimulation of tumor infiltrating lymphocytes) for solid tumors are ongoing in the US and in China.

For more information, please visit http://icellgene.com/

Contact:
Media and Investors
Kevin Pinz
Tel: (631) 538-6218
Kevin.pinz@icellgene.com

News from iCell Gene Therapeutics LLC

iCell Gene Therapeutics, a clinical stage biopharmaceutical company focused on immunotherapies for hematologic malignancies, solid tumors, organ rejections and autoimmune disorders, announced today that it will give oral and poster presentations related to its BCMA-CD19 cCAR and CD4-specific CAR programs at the 61st American Society of Hematology (ASH) Annual Meeting to be held December 7-10, 2019 in Orlando, Florida.

Related link:

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

American Medical Marijuana Physicians Association’s 2019 Annual Meeting Hosted Over 300 Attendees and Physicians

ORLANDO, Fla. /ScoopCloud/ -- The American Medical Marijuana Physicians Association (AMMPA) held their 3rd Annual Conference on October 4-6 at the Hilton Orlando Lake Buena Vista. More than 300 medical marijuana practitioners and physicians from across the nation and other countries around the world attended the 3-day conference.

The meeting provided educational presentations, networking and panel discussions with thought-leaders dedicated to the research and utilization of medical cannabis to improve the health of their patients. AMMPA is the largest medical cannabis association in the world, boasting the highest membership base for an organization of its kind. The AMMPA Annual Conferences are dedicated to medical research and education, presenting on the health benefits of medical cannabis.

This year, the AMMPA Annual Conference featured Keynote Speaker Nikki Fried, the 12th Florida Commissioner of Agriculture and Consumer Services. Commissioner Fried is a strong advocate for medical marijuana and created a Medical Marijuana Advisory Committee this past Summer.

A number of recognized medical marijuana physician leaders attended and over 20 nationally recognized speakers participated in lectures and panel discussions. In addition to Commissioner Fried, our second Keynote Speaker was Professor Hinanit Koltai, PhD, a Senior Research Scientist from the Volcani Center in Israel. Our panel also featured Jade Green, CEO of Jade Green Consulting, an all-female canna-business consultancy, based out of Los Angeles.

The faculty engaged the audience in a series of lectures and panel discussions on the recent literature relevant to the benefits of cannabis in addressing medical conditions such as Cancer, Seizure Disorders, Anxiety, HIV, Chronic Pain, Migraines, and Autism. The Annual Conference was supported by a host of medical cannabis industry leaders including our Premier Emerald Sponsor, Leafly.

About the American Medical Marijuana Physicians Association (AMMPA):
The American Medical Marijuana Physicians Association is a membership driven association, focusing on providing physicians with the resources they need to safely and effectively utilize medical marijuana recommendations as an alternative treatment modality for their patients. AMMPA serves as a physician advocate helping to outline practice risks and benefits, educational requirements, compliance issues, and aggregates its members to allow for a unified voice representing all physicians currently interested in cannabinoid medicine. Our members are leaders in the nation that provide expertise to the public regarding research, education, speaking engagements, seminars, and industry recommendations.

American Medical Marijuana Physicians Association, 1215 E. Robinson Street, Orlando, FL 32801.

Website: https://ammpa.net/

MEDIA ONLY CONTACT:
Savara Hastings
321-917-3212
info@ammpa.net

*PHOTO: https://www.Send2Press.com/300dpi/19-1108s2p-ammpa-event-300dpi.jpg
*Photo Caption - Pictured (L-R): Jade Green, CEO Jade Green Consulting; Savara Hastings, AMMPA Executive Director; Dr. Jaime Snarski, AMMPA Board Member; Megan Zalonka, AMMPA Communications Director.

News from American Medical Marijuana Physicians Association

The American Medical Marijuana Physicians Association (AMMPA) held their 3rd Annual Conference on October 4-6 at the Hilton Orlando Lake Buena Vista. More than 300 medical marijuana practitioners and physicians from across the nation and other countries around the world attended the 3-day conference.

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This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

C Diff Foundation Raises Clostridioides difficile Awareness in St. Louis on Nov. 6-7 at 7th Annual International Conference and Health EXPO

ST. LOUIS, Mo. /ScoopCloud/ -- C Diff Foundation announced today that the 7th Annual International C. diff. Conference and Health EXPO is honored to welcome over 30 international topic-experts dedicated in disciplines of healthcare, pharma, biotech, academia, and Government agencies.

Presenters will deliver data and discuss critical information on a leading Healthcare-Associated Infection (HAI), Clostridioides difficile with global healthcare-associated issues on November 6 - 7, 2019 at the DoubleTree by Hilton Westport Hotel, 1973 Craigshire Road, St. Louis, MO 63146; Telephone: +1 (314) 434-0100.

To learn more about this extraordinary conference, guest speakers, and the diverse topics being presented visit: https://cdifffoundation.org/2019-guest-speakers/

All attendees will have the highest levels of peer networking and learning opportunity at the Conference and Health EXPO.

C Diff Foundation expresses their gratitude to Pfizer for being the conference Diamond Sponsor. Pfizer is appreciated for their continued support and partnering with the C Diff Foundation in promoting C. diff. Awareness worldwide. This activity has been supported by an independent patient advocacy Grant from Merck & Co., Inc., and the members of the C Diff Foundation are truly grateful.

Attendee Paul Feuerstadt MD, FACG, AGAF stated, "The annual C Diff Foundation conference and health expo is an essential conference for me to attend, given the comprehensive presentations about epidemiology, disease state, patient experience, infection control and innovations with treatment of C. difficile. The level of detail and data presented has a wonderful balance that is understandable for someone casually interested in the infection but also exceeds the expectations for those who are experts in the field wanting to share and exchange ideas with other thought leaders."

According to the Centers for Disease Control and Prevention (CDC), Clostridioides difficile infection (aka C. diff., C. difficile, CDI, CDAD) "has become the most common microbial cause of healthcare-associated infections in U.S. hospitals and costs up to $4.8 billion each year in excess health care costs for acute care facilities alone."

Statistics provided by the CDC suggest that C. difficile infections cause nearly 500,000 infections in patients in the U.S. annually. In one study noted by the CDC, among infected patients, nearly 29,000 died within 30 days of being diagnosed, and more than half of those deaths (15,000) were directly attributable to a C. difficile infection.

About The C Diff Foundation:

C Diff Foundation, a 501(c)(3) established 2012, comprised of 100% volunteering professionals is dedicated at supporting public health through education and advocating for Clostridioides difficile infection (CDI) prevention, treatments, clinical trials, AMR, and environmental safety worldwide. Listen to "C.diff. Spores and More" Tuesday's at 1 p.m. EST (www.cdiffradio.com) sponsored by Rebiotix, a Ferring Pharmaceuticals company.

Learn more at: https://cdifffoundation.org/.

Follow C Diff Foundation on LinkedIn, Twitter, Facebook, and Instagram. Twitter @cdiffFoundation #Cdiff2019

Media Contact:
Angelo Ortiz
C Diff Foundation
angelo.ortiz@cdifffoundation.org
Office: (727) 205-3922

*IMAGE link for media: https://www.Send2Press.com/300dpi/19-1015s2p-cdiff-nov-expo-300dpi.jpg

News from C Diff Foundation

C Diff Foundation announced today that the 7th Annual International C. diff. Conference and Health EXPO is honored to welcome over 30 international topic-experts dedicated in disciplines of healthcare, pharma, biotech, academia, and Government agencies. November 6 - 7, 2019 at the DoubleTree by Hilton Westport Hotel.

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This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

BioAdaptives, Inc. Announces Return to Fully Reporting and Appointment of President

LAS VEGAS, Nev. /ScoopCloud/ -- BioAdaptives, Inc. (OTC BB: BDPT) announced the Company's return to a fully-reporting entity, and the appointment of Mr. Robert W. Ellis as its new President, reporting to Dr. Edward E. Jacobs, Jr.

Dr. Jacobs, Director and CEO said, "We are very pleased to again be an SEC fully-reporting Company, even though when it ceased reporting on EDGAR during 2017 and 2018, the Company continued to release full disclosure data via OTC Market's alternate reporting format."

Dr. Jacobs added, "We are also pleased to announce the appointment of Mr. Robert W Ellis to our Management team. With his additional, it allows me the opportunity to spend more time on the strategic development of BioAdaptives, and to continue scientific research and advancement of a broad line of wellness products for people and animals."

"Mr. Ellis brings more than forty years of business management experience to this new assignment. He has held senior financial and operating management positions in aerospace and telecommunication public corporations, as well as private companies in both mature technology business and development-stage entities," Dr. Jacobs further added.

Mr. Ellis stated, "I am pleased to join BioAdaptives in this position and look forward to leading the Company as it emerges further from its development stage and matures into a growing successful manufacturing and distribution company. We expect to expand BioAdaptives operation through acquisitions and subsidiary entities in its current natural wellness sphere and in related fields in order to add to the Company's bottom line."

About BioAdaptives, Inc.:

BioAdaptives, Inc. is a fully-reporting, public company trading on the OTC Bulletin Board under the symbol BDPT. The company is engaged in research and development in science-based nutraceutical products for human and animal consumption. Learn more at: https://bioadaptives.com/.

SAFE HARBOR ACT:

Forward-Looking Statements: This release contains statements that constitute forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements appear in a number of places in this release and include all statements that are not statements of historical fact regarding the intent, belief or current expectations of BioAdaptives, Inc. and its directors or its officers with respect to, among other things: (i) financing plans; (ii) trends affecting its financial condition or results of operations; (iii) growth strategy and operating strategy. The words "may," "would," "will," "expect," "estimate," "can," "believe," "potential" and similar expressions and variations thereof are intended to identify forward-looking statements. Investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, many of which are beyond BioAdaptives, Inc.'s ability to control, and actual results may differ materially from those projected in the forward-looking statements as a result of various factors. More information about the potential factors that could affect the business and financial results is and will be included in BioAdaptives, Inc.'s filings with the Securities and Exchange Commission.

Ticker: OTCBB:BDPT / OTC:BDPT / OP: BDPT

News from BioAdaptives Inc.

BioAdaptives, Inc. (OTC BB: BDPT) announced the Company's return to a fully-reporting entity, and the appointment of Mr. Robert W. Ellis as its new President, reporting to Dr. Edward E. Jacobs, Jr.

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This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

2019 Lupus Insight Prize Awarded to Dr. Ignacio Sanz: Recognizes Studies of Harmful Immune Cells in Lupus

BOSTON, Mass. /ScoopCloud/ -- The Lupus Research Alliance has awarded its 2019 Lupus Insight Prize to Ignacio Sanz, MD, for discovering that certain little-understood immune system cells are a major source of the harmful proteins that promote lupus symptoms. His work could spark new treatments for the disease and help doctors determine which patients could benefit from current drugs. Dr. Sanz is a Mason Lowance Professor of Medicine and Pediatrics and Chief of the Division of Rheumatology at Emory University School of Medicine in Atlanta, Georgia.

The award was announced June 19 at FOCIS 2019, the 19th Annual Meeting of the Federation of Clinical Immunology Societies (FOCIS). The $100,000 award recognizes a major, novel insight and/or discovery with the promise of changing thinking about lupus as well as a high probability of generating further advances in the diagnosis and treatment of the disease.

"Dr. Sanz has already made vital contributions to understanding the role of B cells in lupus," said Kenneth M. Farber, President and CEO, Lupus Research Alliance. "We very much look forward to his next advances afforded by our Lupus Insight Prize."

Dr. Sanz's discoveries were a breakthrough for understanding how certain B cells, a type of immune cell, promote lupus. B cells are key for the disease. Their normal job is to produce proteins called antibodies that protect against bacteria and viruses. But in lupus, B cells release antibodies that trigger damage to patients' own tissues. Researchers have known that some B cells must mature in specialized parts of the lymph nodes or spleen before they can make these destructive antibodies.

Dr. Sanz showed that many damaging B cells follow a different route and identified the molecular mechanisms that underpin this B cell activation pathway. He and his team were the first to apply a comprehensive characterization of these cells using cutting-edge techniques such as multidimensional flow cytometry analysis of DNA in lupus patients. They found that this group of B cells was prevalent in patients who were undergoing lupus flares, particularly African-Americans. Dr. Sanz and his colleagues also found that, in contrast to healthy subjects, the lupus B cells were ready to transform into cells that produce harmful antibodies, even in patients without active disease.

"I thank the Lupus Research Alliance for recognizing my work, and I am eager to pursue further research with the potential for improving patient treatment," said Dr. Sanz.

Researchers may be able to build on Dr. Sanz' discoveries to develop new drugs that could reduce patients' risk and severity of disease flares. The results could also help doctors identify subsets of lupus patients that are more likely to benefit from therapies that destroy B cells using existing drugs. In addition, the cellular and molecular make-up of the abnormal lupus B cells should help identify new therapeutic targets.

About Lupus

Lupus is a chronic, complex autoimmune disease that affects millions of people worldwide. More than 90% of people with lupus are women; lupus most often strikes during the childbearing years of 15-45. African Americans, Latin Americans, Asians and Native Americans are two to three times at greater risk than Caucasians. In lupus, the immune system, which is designed to protect against infection, creates antibodies that can attack any part of the body including the kidneys, brain, heart, lungs, blood, skin, and joints.

About the Lupus Research Alliance

The Lupus Research Alliance aims to transform treatment while advancing toward a cure by funding the most innovative lupus research in the world. The organization's stringent peer review grant process fosters diverse scientific talent who are driving discovery toward better diagnostics, improved treatments and ultimately a cure for lupus. Because the Lupus Research Alliance's Board of Directors funds all administrative and fundraising costs, 100% of all donations goes to support lupus research programs.

Learn more at: https://www.lupusresearch.org/

News from Lupus Research Alliance

The Lupus Research Alliance has awarded its 2019 Lupus Insight Prize to Ignacio Sanz, MD, for discovering that certain little-understood immune system cells are a major source of the harmful proteins that promote lupus symptoms. His work could spark new treatments for the disease and help doctors determine which patients could benefit from current drugs.

Related link:

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

C Diff Foundation Recognizes Rebiotix CEO with 2019 ‘Above and Beyond’ Award

NEW PORT RICHEY, Fla. /ScoopCloud/ -- The C. Diff Foundation Board of Directors announced today that the 2019 "Above and Beyond" Award will be presented to Rebiotix CEO Lee Jones in Roseville, Minnesota. The award, given to one recipient annually, is given to a person or organization that show extraordinary dedication to C. diff patient safety, advocacy, and overall drive to improve the lives of those impacted by the infection.

"We are very proud to recognize Ms. Jones with our "Above and Beyond" award," said C. Diff Foundation Founder and President, Nancy Caralla. "Lee's dedication to the entire C. diff community of patients, family members, and physicians hasn't wavered since the founding of Rebiotix in 2011. She is a true example of what can happen when focusing on patient well-being drives new approaches to healthcare."

The award will be presented by the Foundation's Vice President, Scott Battles, and Treasurer Angelo Ortiz at the Rebiotix facility.

"It's an honor to receive this award from the C. Diff Foundation," said Ms. Jones. "The purpose of starting Rebiotix was to bring the power of the microbiome to the clinic in a scientifically sound, quality-controlled way to help patients. We stand with the Foundation in believing that patient well-being should be at the core of all that we do, from clinical trials to exploring new scientific landscapes within the microbiome space."

About the C Diff Foundation:

The C Diff Foundation is a non-profit, 501(c)(3) organization established in 2012. It is comprised of 100% volunteering professionals dedicated to supporting public health through education and advocacy for C. difficile infection prevention, treatments, environmental safety and support world-wide. The Foundation's CEO and founder is a nurse inspired to create the foundation after witnessing the loss of her father to CDI, as well as suffering from the infection herself. The C Diff Foundation members, with their volunteer patient advocates, successfully "raise C. diff awareness" locally and in over fifty-six (56) countries and host a U.S. nation-wide hotline (1-844-FOR-CDIF) to support healthcare providers, patients and families through the difficulties of a C. diff infection. Learn more: https://cdifffoundation.org/

About Rebiotix Inc.:

Rebiotix Inc., part of the Ferring Pharmaceuticals Group, is a late-stage clinical microbiome company focused on harnessing the power of the human microbiome to revolutionize the treatment of debilitating diseases. Rebiotix possesses a deep and diverse clinical pipeline, with its lead drug candidate, RBX2660, in Phase 3 clinical development for the prevention of recurrent Clostridium difficile (C. diff) infection. RBX2660 has been granted Fast Track, Orphan and Breakthrough Therapy designation from the FDA for its potential to prevent recurrent C. diff infection.

Rebiotix's clinical pipeline also features RBX7455, a lyophilized, room temperature stable oral capsule formulation. Rebiotix is also targeting several other disease states with drug products built on its pioneering Microbiota Restoration Therapy(tm) platform. For more information on Rebiotix and its pipeline of human microbiome-directed therapies, visit https://www.rebiotix.com/

Twitter: @cdiffFoundation #CdiffInfection #Clostridiumdifficile @Rebiotix

News from C Diff Foundation

The C. Diff Foundation Board of Directors announced today that the 2019 "Above and Beyond" Award will be presented to Rebiotix CEO Lee Jones in Roseville, Minnesota. The award, given to one recipient annually, is given to a person or organization that show extraordinary dedication to C. diff patient safety, advocacy, and overall drive to improve the lives of those impacted by the infection.

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Pet King Brands Celebrates 20 Years as a Leader in the Pet Health Products Industry

WESTMONT, Ill. /ScoopCloud/ -- Pet health products company, Pet King Brands, Inc. - the maker of veterinarian-recommended brands ZYMOX(R) Dermatology and Oratene(R) Brushless Oral Care - celebrates 20 years of helping pets find relief from problematic ear, skin and mouth conditions.

This is a major milestone in the history of the woman-founded and -owned company and signifies the importance of offering pet owners and pet healthcare professionals alternatives to antibiotics and harsh chemicals to aid in the management of some of the most common health issues affecting the majority of pets.

Founded in 1998 by Pamela K. Bosco, Pet King Brands utilizes its patented LP3 Enzyme System in all of its solutions from ear products to skin topicals to shampoo and conditioning rinse and brushless oral care products. All of Pet King Brands' products are manufactured in the United States.

"Twenty years ago, the issues of drug-resistant health conditions in people and animals were just starting to be talked about," said Bosco, President and founder of Pet King Brands. "As a result, people started to search for a healthier, more effective alternative for their own and their pet's healthcare."

Pet King Brands began with three products and now provides a full spectrum of topical dermatological products for problematic ears and skin - available with or without added hydrocortisone - as well as a full line of oral care products that don't require brushing to be effective. Since first being introduced through veterinarian clinics nationwide, Pet King Brands has distributed over 1 million bottles of its flagship product ZYMOX(R) Otic Ear Solution and continues to expand its pet health products line.

In addition to veterinarian clinics across the country, Pet King Brands' ZYMOX(R) and Oratene(R) products are available in pet specialty stores and through online retailers.

"It's always been our mission to provide solutions, but first, do no harm. Our enzymatic solutions represent cutting-edge technology without the side effects associated with antibiotics," added Bosco. "We are very proud to not have deviated from our mission since we started 20 years ago but more so, we are so thankful that ZYMOX and Oratene have had such a positive impact on the comfort and health of so many pets across the country."

About Pet King Brands, Inc.

Pet King Brands is led by President and Founder, Pamela Bosco, who first introduced ZYMOX to the veterinary world in 1998. Based on years of research, she knew she had a product that was going to change the way people managed pet ear infections. Pet King Brands' patented LP3 Enzyme System is used in the most complete and complex enzymatic dermatology and oral care products available on the market for both small and large animals.

Its ZYMOX Dermatology products remain a stark contrast to other products on the market, offering effective solutions that are easy to use, free of harsh chemicals and antibiotics, and made in the United States. In addition to its skin topicals, Pet King Brands' product family includes ear care products, brushless oral care products, shampoos and conditioning rinses.

The ZYMOX and Oratene lines represent true advances in the field of veterinary healthcare. Bosco owes her discovery to her brother, Michael Pellico, the bioscientist credited with adapting his enzyme technology in Biotene(R) - the #1 dentist-recommended product for people suffering from Dry Mouth and owned by GlaxoSmithKline - and making it safe for use in animals. Pet King Brands' unwavering commitment to the well-being of animals is the reason they take such great pride in delivering high-quality products that are safe as well as effective. ZYMOX and Oratene are available through veterinarians and select retailers.

To learn more visit https://www.zymox.com/.

News from Pet King Brands

Pet health products company, Pet King Brands, Inc. - the maker of veterinarian-recommended brands ZYMOX(R) Dermatology and Oratene(R) Brushless Oral Care - celebrates 20 years of helping pets find relief from problematic ear, skin and mouth conditions.

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This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of and © the Neotrope® News Network - all rights reserved.

Paragon BioTeck, Inc. Hosts Pearl Buck Preschool Holiday Event

PORTLAND, Ore. /ScoopCloud/ -- Paragon BioTeck announces holiday event, "A Night to Remember," scheduled Friday, Dec. 7, 2018 from 5:30 - 8 p.m. in Eugene, Ore. The event delivers a magical night of holiday sights and sounds for the families of Pearl Buck Preschool.

"The work of Pearl Buck Center resonates with us," said Patrick Witham, President and CEO of Paragon BioTeck. "We are motivated by their dedication to ensuring that people with disabilities have the right to participate in all aspects of life, in their community and the workplace. We are inspired by their innate ability to see an individual's strengths, not deficits, ability not disability.

"We are proud to support organizations that enrich the lives of children and families who defy incredible challenges presented to them, and we are looking forward to celebrating another incredible 'Night to Remember' with the families of Pearl Buck."

WHEN: Friday, Dec. 7, 2018, 5:30 p.m. - 8 p.m.
Santa appearance at 6:45 p.m.

WHERE: Pearl Buck Center, 3690 West 1st Ave, Eugene, OR 97402

WHAT: "A Night to Remember," an evening of holiday cheer features special appearances by Santa, and The Duck from University of Oregon before the children embark on a tour of holiday lights. Santa's reindeer will also attend the event. Dinner, hot cocoa and treats will be provided by local McDonald's and Dutch Bros. Coffee.

WHO: Children and families of the Pearl Buck Preschool, a tuition-free Pearl Buck Center program providing education and early-age development tailored to families led by parents with cognitive challenges.

About Paragon BioTeck, Inc., and Paragon Gives:
Paragon BioTeck, Inc. is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies. Paragon Gives supports a number of charities and organizations within the biotechnology and health care arena, as well as individuals and organizations that have made a positive impact on the employees, customers, and partners of Paragon BioTeck.

Learn more about Paragon BioTeck at https://paragonbioteck.com .

About the Pearl Buck Center Preschool & Family Supports Program:
Founded in 1953, Pearl Buck Center in Eugene, Ore., provides support to people with disabilities and their families. The Pearl Buck Preschool & Family Supports Program provides a specialized preschool for children whose parents have cognitive challenges, and includes case management and parent mentoring.

Learn more about Pearl Buck Center at https://pearlbuckcenter.com.

News from Paragon BioTeck, Inc.

Paragon BioTeck announces holiday event, "A Night to Remember," scheduled Friday, Dec. 7, 2018 from 5:30 - 8 p.m. in Eugene, Ore. The event delivers a magical night of holiday sights and sounds for the families of Pearl Buck Preschool.

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Leading Companies to Support C Diff Foundation 6th Annual International C.diff. Conference and Health EXPO, Nov. 8-9, Philadelphia

PHILADELPHIA, Pa. /ScoopCloud/ -- The C Diff Foundation is honored to welcome leading companies to the 6th Annual International "C.diff. Awareness Conference and Health EXPO," as they come together to make a global difference. These companies are dedicated to the prevention, diagnostics, treatments, environmental safety products and services focused on C.difficile infections and Healthcare-associated infections and whose role serves great importance in the C.diff. community.

The conference takes place on November 8 and 9, 2018 at the Embassy Suites by Hilton Philadelphia Airport Hotel, Philadelphia, Pennsylvania.

"We at Synthetic Biologics are thrilled to partner with the C Diff Foundation in their fight to increase research partnerships, education and advocacy of awareness of Clostridium difficile Infection," said Deb Mathews, PharmD, Vice President, Medical Affairs of Synthetic Biologics. "This conference consistently brings the highest caliber of speakers, rigorously sound clinical data, an impassionate approach and an unyielding commitment in the fight against the incredible unmet medical needs for patients inflicted with and affected by Clostridium difficile Infection."

According to the Centers for Disease Control and Prevention (CDC), Clostridium difficile infection "has become the most common microbial cause of healthcare-associated infections in U.S. hospitals and costs up to $4.8 billion each year in excess health care costs for acute care facilities alone." Statistics provided by the CDC suggest that C. difficile cause nearly 500,000 infections in patients in the U.S. annually and 14,000 deaths a year directly related to this infection.

The 6th Annual International C. diff. Conference & Health EXPO brings together C. diff survivors, physicians, researchers and industry members focused on reducing the major burden of C. difficile infection on global healthcare systems.

"We're privileged to be able to present alongside distinguished C. difficile infection experts and to share with the community our progress on advancing our Phase 3-ready precision antibiotic ridinilazole as a potential new front-line treatment option for patients with C. difficile infection," said Dr. David Roblin, President of R&D of Summit Therapeutics.

With upmost appreciation we thank the following Sponsors for their continued support and partnering with the C Diff Foundation promoting C. diff. awareness worldwide:
- Diamond: Synthetic Biologics.
- Gold: Clorox Healthcare, Seres Therapeutics, ROCHE, Rebiotix, Pfizer.
- Silver: CutisPharma, TechLab, Tru-D Smart UVC, Summit Therapeutics.
- Bronze: Honey Bee Handiworks, Qmetis, Seal Shield, Trinity Guardion, Steriliz RD Rapid UVC, Safety Net America, SporeGen.
- Luncheon: Finch Therapeutics, Synexsis.
- A/V - DaVolterra.

This conference is supported through an educational grant from Sanofi Pasteur US. This activity has been supported by an independent patient advocacy grant from Merck & Co., Inc.

About The C Diff Foundation:

The C Diff Foundation, a 501(c)(3) established 2012, comprised of 100% volunteering professionals dedicated at supporting public health through education and advocating for C. difficile infection (CDI) prevention, treatments, clinical trials, environmental safety, and support worldwide. https://cdifffoundation.org/.

Follow C Diff Foundation on Facebook, Instagram.

Twitter @cdiffFoundation #Cdiff2018

News from C Diff Foundation

The C Diff Foundation is honored to welcome leading companies to the 6th Annual International "C.diff. Awareness Conference and Health EXPO," as they come together to make a global difference. These companies are dedicated to the prevention, diagnostics, treatments, environmental safety products and services focused on C.difficile infections and Healthcare-associated infections and whose role serves great importance in the C.diff. community.

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Healthcare Tech Outlook Names Delta Care Rx a Top 10 Pharmacy Management Solution Provider

FREMONT, Calif. /ScoopCloud/ -- Delta Care Rx, a leading pharmaceutical innovator in end of life care, has been named one of the "Top 10 Pharmacy Management Solution Providers of 2018," according to Healthcare Tech Outlook, a digital and print magazine publication of Valley Media, Inc.

The "Top 10" award was published online March 27, as well as in a Special Issue print edition on April 5, with Delta Care Rx Founder, President, and COO Drew Mihalyo on its cover. Mihalyo, known for his commitment to technological innovation providing unique programs for hospice customers exclusively offered by Delta Care Rx, is quick to share the credit for the company's success.

"This recognition is a testament to the strength and commitment of the entire Delta Care Rx team," says Mihalyo. "We work together, both within Delta and with our integration partners, to ensure prompt attention and great sensitivity to meet each patient's needs related to pain and symptom management."

The in-depth feature article, "Delta Care Rx: Enhancing the End of Life Care Experience," states that the company "sets the industry benchmark in pharmaceutical benefits management in end of life care," fulfilling its mission of transparency and commitment to quality of care at every level of the organization. In addition to providing benefit management or mail order pharmacy to clients, Delta Care Rx offers a range of cutting edge telemedicine solutions designed to simplify workflow and ordering processes and improve quality of care. The article places these within the context of the broader pharmaceutical and end of life care industries.

"We take pride in honoring Delta Care Rx for offering innovative solutions that are revolutionizing the way hospice and palliative care providers are served in the Pharmacy Management arena," said Alex D'Souza, managing editor of Healthcare Tech Outlook.

With the announcement, Delta Care Rx joins an elite group of pharmacy management solutions providers known to provide innovative technologies which ultimately enhance clinical efficiency and dramatically reduce costs for hospice organizations. The magazine's editorial board independently applied a set of criteria to a broad selection of pharmacy management firms, then narrowed the designation to the Top 10 listing.

Delta Care Rx - http://www.deltacarerx.com/ - transforms and improves the hospice pharmacy industry through business transparency, innovation, extreme customer service, and the maintenance of vital community pharmacy relationships.

About Delta Care Rx:

As a pharmacist owned, privately held provider, Delta Care Rx - http://www.deltacarerx.com - sets the industry benchmark for pharmacy benefit management, creative prescription mail order, on-demand pharmacist services, and hospice tailored e-Prescribing. Additionally, Delta Care Rx offers electronic tools, including cutting-edge telemedicine technology, to improve the quality of palliative patient care during serious illness or at end of life and simplifies essential workflow/ordering processes within hospice settings.

About Healthcare Tech Outlook:

Published from Fremont, California, Healthcare Tech Outlook is a print magazine, which features CIOs, ITVPs, CTOs, and other decision makers sharing their insights and perspective on healthcare industry. A panel of experts, technology leaders and board members of Healthcare Tech Outlook magazine has finalized the "Top 10 Pharmacy Management Solution Providers 2018" and shortlisted the best vendors and consultants in the healthcare industry. For more info, visit: https://www.healthcaretechoutlook.com/.

News from Delta Care Rx

Delta Care Rx, a leading pharmaceutical innovator in end of life care, has been named one of the "Top 10 Pharmacy Management Solution Providers of 2018," according to Healthcare Tech Outlook, a digital and print magazine publication of Valley Media, Inc.

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Alejandro Arboleda Named 2018 Koch Kellan Scholar

PORTLAND, Ore. /ScoopCloud/ -- Paragon BioTeck, Inc., an ophthalmic pharmaceutical and medical device company, announced today that Alejandro Arboleda has been named its 2018 Koch Kellan Scholar. Paragon Gives, a Paragon BioTeck initiative, awards the Koch Kellan Scholarship to an outstanding graduate medical student committed to elevating the standard of eye care through social responsibility and a clinical, teaching or research career in ophthalmology.

Patrick Witham, President and CEO of Paragon BioTeck, discussed the importance of the scholarship in regard to ophthalmology, "Since its inception, this award has been extended to some of the best and brightest up and coming stars in this area of medicine. The award's namesake is perfectly apt, given the unparalleled caliber of candidates and recipients that have shown interest in pursuing a career in an area of medicine where both Dr. Koch and Dr. Kellan have made such tremendously important contributions."

Witham added, "While the contributions they have made to restoring sight in and of itself is remarkable, it is their vision that they so generously share that will leave their indelible mark on countless lives well beyond our time."

Both Robert Kellan, MD and Paul Koch, MD, spoke of Mr. Arboleda's determination to pursue a career in ophthalmology. "While many students imagine how things ought to be and wonder why not, Alejandro stepped out where few others do. He took actions to accomplish changes in the world around him. I have no doubt he has the temperament and the drive to accomplish many wonderful things and change our world as we know it," Koch stated.

Mr. Arboleda is a third-year student at the University of Miami Miller School of Medicine. His initial studies in biomedical engineering drove his interest in ophthalmology. "I was not satisfied by simply creating novel devices, I wanted to be the physician with the experience to face problems and invent better solutions to treat patients," he said. After collaborating with researchers in France during his tenure as a Fulbright Fellow, he began a photodynamic therapy (PDT) project.

Kellan noted Mr. Arboleda's passion for caring for those in need, "Alejandro clearly demonstrates his compassion to make the world a better place by his eager participation in ophthalmic mission trips to South America and his tireless efforts to bring visual rehabilitation to the needy."

Mr. Arboledo expressed how these experiences reaffirmed his dedication to medicine, "I have followed each patient's journey and am humbled by their reactions to their recovery."

Upon receipt of the award, Mr. Arboleda discussed how the scholarship mirrors both his commitment to driving innovation and serving the population, "I feel very honored to receive the Koch Kellan Scholarship. I look forward to dedicating my career to the field of ophthalmology where there is so much space for advancement and serving diverse patient populations. I will continue to work hard so that my contributions to the field of ophthalmology honor the spirit of this award."

Paragon Gives will formally present the Koch Kellan Scholarship to Mr. Arboleda at a dinner attended by scholarship namesakes, Drs. Koch and Kellan, and Paragon CEO, Patrick Witham, during the annual meeting of the American Society of Cataract and Refractive Surgery, held April 14-17, 2018 in Washington D.C.

About Paragon Gives and the Koch Kellan Scholarship:

Paragon Gives, a Paragon BioTeck, Inc., initiative, supports a number of charities and organizations, including those within the biotechnology and health care arena. The initiative also works with individuals and organizations that have made a positive impact on our customers, vendors, investors and industry as a whole.

The Koch Kellan Scholarship affirms Paragon's commitment to elevating the standard of eye care and enhancing patient quality of life. Alejandro Arboleda is the fourth recipient of the scholarship. Previous recipients include Xinxin Zhang of the University of North Carolina, Chapel Hill, and Hasenin Al-khersan of the University of Chicago Pritzker School of Medicine. The scholarship was first awarded to Captain Edward Woodward of the University of South Florida Morsani College of Medicine in 2015.

Learn more at: https://paragonbioteck.com/gives/kochkellan/.

About Paragon BioTeck, Inc.:

Paragon BioTeck, Inc., is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies. Paragon BioTeck's portfolio of products is designed to protect and preserve eyesight and deliver comfort to the eyes.

Learn more at: https://paragonbioteck.com/.

News from Paragon BioTeck, Inc.

Paragon BioTeck, Inc., an ophthalmic pharmaceutical and medical device company, announced today that Alejandro Arboleda has been named its 2018 Koch Kellan Scholar. Paragon Gives, a Paragon BioTeck initiative, awards the Koch Kellan Scholarship to an outstanding graduate medical student committed to elevating the standard of eye care through social responsibility and a clinical, teaching or research career in ophthalmology.

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C Diff Foundation Presents Award to CutisPharma in Recognition of Contribution to C. diff. Community

NEW PORT RICHEY, Fla. /ScoopCloud/ -- The C Diff Foundation announced today that it presented CutisPharma, Inc., its "Making a Difference" award as a special recognition of the significant contribution that CutisPharma has made to the C.diff. Community: helping the advancement of C.diff. awareness as well as expanding treatment options for C.diff. patients.

The award was presented at CutisPharma's celebration of its upcoming launch of FIRVANQ(TM), recently approved by the FDA for the treatment of Clostridium difficile associated diarrhea and enterocolitis caused by Staphylococcus aureus, including methicillin-resistant strains. Upon launch, FIRVANQ(TM) will be the only FDA-approved oral vancomycin solution treatment commercially available, improving patient access and reducing pharmacist burden by no longer having to compound oral liquid formulations.

"CutisPharma has been a committed partner of our Foundation and has furthered our mission to increase C.diff. awareness and support the research and development of new treatment options," said Nancy C. Caralla, Foundress and Executive Director of the C Diff Foundation. "In recognition of CutisPharma's efforts, we are pleased to grant them the 'Making a Difference' award at this special moment in the Company's 20th anniversary year."

"We are very grateful to receive such a special distinction from the C Diff Foundation," said Neal I. Muni, MD, MSPH, and Chief Executive Officer of CutisPharma. "For 20 years, we have been committed to improving the lives of patients who are not well-served by existing therapies and would benefit from high-quality, cost-effective new treatment options. We greatly value our partnership with the C Diff Foundation and look forward to continuing to support their mission."

In the USA: Nearly half a million Americans suffer from Clostridium difficile (C. diff.) infections in a single year according to a study released in 2015 by the Centers for Disease Control and Prevention (CDC). Approximately 29,000 patients died within 30 days of the initial diagnosis of C. difficile. Of those, about 15,000 deaths were estimated to be directly attributable to C. difficile infections making C. difficile a very important cause of infectious disease death in the United States.

About the C Diff Foundation:

The C Diff Foundation, a 501(c)(3)non-profit organization, established in 2012, is comprised of 100 percent volunteering professionals dedicated to supporting public health initiatives for C. difficile infection prevention, treatments, environmental safety, and support worldwide. For more information, visit: https://cdifffoundation.org/.

About CutisPharma:

CutisPharma, Inc., based in Wilmington, Mass., is privately held, specialty pharmaceutical company that has been the industry leader for 20 years in providing innovative solutions to pharmacists. CutisPharma's FIRST(r) Unit-of-Use Compounding Kits have benefited millions of patients who are unable to swallow conventional oral dosage forms such as tablets and capsules and whose needs are not served by commercially available therapies. The Company's first FDA-approved Kit, FIRVANQ(TM), will allow significantly broader patient access, convenience to pharmacists and patients alike by reducing the need for compounding, and serve as a potential cost-saving option to existing treatments. For more information, visit: https://cutispharma.com/.

News from C Diff Foundation

The C Diff Foundation today announced that it presented CutisPharma, Inc., its "Making a Difference" award as a special recognition of the significant contribution that CutisPharma has made to the C.diff. Community: helping the advancement of C.diff. awareness as well as expanding treatment options for C.diff. patients.

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Delta Care Rx Now Integrates with Suncoast Electronic Medical Records

PITTSBURGH, Pa. /ScoopCloud/ -- Delta Care Rx, a leading pharmaceutical innovator in end of life care, announces a robust integration with Suncoast by Complia Health, a leading global provider of home health care and hospice software solutions.

The Delta Care Rx hospice pharmacy benefits management (PBM) solution joins a growing list of other vendors which integrate effortlessly with the Suncoast industry standard electronic medical records (EMR) system. Now, clients with the Suncoast EMR are able to enhance efficiencies with a single point of data entry which will then flow electronically to Delta Care Rx.

"The integration allows an increased number of our clients to use the additional functionality of the software," says Nate Truitt, general manager of Suncoast by Complia Health. "We want to make certain our clients have access to all the software options available to them."

The integration:
* increases efficiency, saving time and costs
* eliminates redundancy of any data entry
* improves the quality of patient care
* provides a single point of entry for patient demographics and medication orders
* complements Delta Care Rx's proprietary and easy-to-use e-Tools suite of software.

The integration is inclusive of industry tailored e-Prescribing and durable medical equipment (DME) order management that works on any digital device, including smart phones.

A leading PBM, Delta Care Rx partners with top EMR vendors - like Suncoast by Complia - to provide innovative integration solutions which ultimately enhance clinical efficiency and dramatically reduce costs for hospice organizations.

According to David Clapp, national director of business development at Delta Care Rx, "We appreciate the opportunity to partner with quality providers like Suncoast by Complia. Together, we make it possible for our mutual clients to ensure patient quality of care across the care continuum."

Delta Care Rx is a leading sponsor for the second annual Complia Health CARE User Conference, Monday, Feb. 19, through Friday, Feb. 23, 2018 at the Marriott Orlando World Center, Orlando, Florida.

Attendees will network with peers in post-acute, home health, hospice and palliative care organizations, while simultaneously learning from a broad variety of industry experts and thought leaders, such as Delta Care Rx COO Drew Mihalyo, who will be featured in Thursday's Partner Showcase.

About Delta Care Rx:
Delta Care Rx - http://www.deltacarerx.com - transforms and improves the hospice pharmacy industry through business transparency, innovation, extreme customer service, and the maintenance of vital community-pharmacy relationships. As a pharmacist owned, privately held provider, Delta Care Rx sets the industry benchmark for pharmacy benefit management, mail order pharmacy options, on-demand pharmacist services, and hospice tailored electronic prescribing. Additionally, Delta Care Rx offers electronic tools, including cutting edge telemedicine technology, to improve the quality of patient care and simplify essential workflow and ordering processes within hospice settings.

About Complia Health:
Complia Health is a leading global provider of technology and expertise for the long-term and post-acute care market. Nearly 3,000 home health, residential, community care, and hospice organizations count on Complia Health for the clinical, operational, and financial solutions required to profitability deliver quality care. Complia Health's innovative products-including Procura, ContinuLink, Suncoast, Igea, and Progresa-are supported by a team of global health and technology experts located in the United States, Canada, and Australia. For more information, visit http://www.compliahealth.com/.

News from Delta Care Rx

Delta Care Rx, a leading pharmaceutical innovator in end of life care, announces a robust integration with Suncoast by Complia Health, a leading global provider of home health care and hospice software solutions.

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ScriptDrop and Albertsons Hurricane Relief Efforts To Be Covered on ‘The Success Files’ with Rob Lowe

NASHVILLE, Tenn. /ScoopCloud/ -- ScriptDrop, a healthcare technology company providing medication reminders and deliveries while fighting prescription abandonment and abuse, today announced that it will be featured on "The Success Files" hosted by Rob Lowe, airing on MSNBC and PBS in 2018.

The segment will show how ScriptDrop teamed up with Albertsons Companies to provide relief to Hurricane Harvey victims prevented from picking up their prescriptions in the aftermath of the storm. "We're delighted that 'The Success Files' decided to tell the story of how technology helped to alleviate at least some of the pressure on families in need," said ScriptDrop CEO Nicholas Potts.

"After Hurricane Harvey, we had patients who were struggling to meet their basic needs, so partnering with ScriptDrop to deliver their prescriptions to their homes was an easy decision and allowed our patients to stay healthy and focus on recovery efforts," says Mark Panzer, Albertsons Companies Senior Vice President of Pharmacy Health and Wellness.

"Our data showed that people were either unable to reach the pharmacy or dealing with other priorities," added ScriptDrop's Potts. "By offering our expertise in prescription delivery with Albertsons Companies, we could help people by bringing prescriptions to them and assisting with copays." Albertsons stepped in to cover the cost of the deliveries and the copays were paid for by funds raised.

"The Success Files" is an award-winning program that highlights new stories and innovative concepts through groundbreaking short-form and long-form documentary presentation. The hurricane provided an opportunity for ScriptDrop to test its systems in a high pressure environment. ScriptDrop connects patients, pharmacies and physicians to ensure that patients properly adhere to medication protocols prescribed by their physicians, and that healthcare providers and pharmacies are informed if there are problems.

The complex system or reporting and notifications is implemented through the use of cutting edge blockchain technology, ensuring both the security and accuracy of the process.

The Success Files will tape the segment in Houston on November 14, and it will run on MSNBC and PBS stations throughout 2018.

About ScriptDrop:

ScriptDrop offers a prescription delivery service that makes the delivery process easier for both pharmacists and patients. Once a prescription is ready, ScriptDrop sends a courier to pick up the delivery and tracks the delivery until the patient signs for it. The pharmacist can then view the signed delivery receipt in their ScriptDrop account. ScriptDrop is designed to fit into the pharmacist's workflow, enabling patients to have easy access to medicines and pharmacists to streamline processes as well as access reporting and analytical insight.

Learn more at: http://www.scriptdrop.co/.

Media Contact
Nicholas Potts
Email: nick@scriptdrop.co
Tel: 615-522-7117

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News from ScriptDrop

ScriptDrop, a healthcare technology company providing medication reminders and deliveries while fighting prescription abandonment and abuse, today announced that it will be featured on "The Success Files" hosted by Rob Lowe, airing on MSNBC and PBS in 2018.

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ECHO Connection – Cannabinoid-Based Education, Collaboration and Hope – Non-Profit Charitable Org Appoints New CEO Andrea Barnes

SAN DIEGO, Calif. /ScoopCloud/ -- ECHO Connection, a non-profit charitable organization dedicated to educating the world, hosting collaborative platforms, and providing hope for those in need of cannabinoid-based therapies, announced today that it has appointed Andrea Barnes as its new CEO and President. ECHO Connection also announced that Barnes will be speaking about the charity's work in guiding families seeking the therapeutic effects of cannabinoids by connecting them with resources that can help at the 4th Annual Cannabis World Congress & Business Exposition (CWCBE) in Boston, Massachusetts on Thursday, October 5 at 10 a.m.

Barnes brings more than 30 years of experience leading local, national and international causes to her new role as ECHO Connection's CEO and President. Currently, Barnes also serves as CEO of the corporate philanthropy, fundraising and education consulting company The Giving Principles.

"I am excited to be taking on this new leadership role at ECHO Connection to help the organization deliver on its mission of changing lives with cannabinoid therapies," Barnes said. "My personal mission is to create unprecedented support for good in the world.

"I am extremely impressed by what ECHO Connection has accomplished thus far in providing families with loved ones suffering with debilitating neurological disorders such as epilepsy, autism, and other conditions with financial assistance, medical referrals, and access to cannabinoid products all through charitable donations."

Barnes will be speaking on the "Patient and Caregiver" panel at the CWCBE at 10 a.m. on Thursday, October 5 at the John Hynes Convention Center in Boston about how ECHO Connection is providing support for special case families that count on cannabinoids.

Barnes has also served as the Executive Director of the MORE Project, Senior Vice President for Globus Relief, Director of Development for the Waterford School, and General Manager of the Gina Bachauer International Piano Foundation. She holds a bachelor's and master of fine arts degree from the University of Utah.

ECHO Connection strives to impact the world through three comprehensive programs:
EDUCATION - Learn about the medical benefits of cannabinoids.

COLLABORATION - Join a growing cannabinoid community.

HOPE - Provide relief to families suffering from serious medical conditions.

About ECHO Connection:
ECHO Connection is a 501(c)(3) nonprofit charitable organization dedicated to supplying cannabinoid-based education, open-ended collaboration between doctors and patients, and hope to families facing serious medical conditions.

Learn more at https://echoconnection.org/.

Follow us on social media:
Facebook - https://www.facebook.com/myechoconnection/

Twitter - https://twitter.com/echoconnection1

Information on the 4th Annual Cannabis World Congress and Business Exposition: http://www.cwcbexpo.com/overview-boston-2017/

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News from ECHO Connection

ECHO Connection, a non-profit charitable organization dedicated to educating the world, hosting collaborative platforms, and providing hope for those in need of cannabinoid-based therapies, announced today that it has appointed Andrea Barnes as its new CEO and President. Barnes will be speaking about the charity's work in guiding families seeking the therapeutic effects of cannabinoids by connecting them with resources that can help at the 4th Annual Cannabis World Congress & Business Exposition (CWCBE) in Boston.

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Paragon BioTeck Calls Emerging Leaders to Apply for 2018 Ophthalmology Scholarship

PORTLAND, Ore. /ScoopCloud/ -- Paragon BioTeck, Inc., a privately-held pharmaceutical and medical device company, today announced the call for the next Koch Kellan Scholar. The annual Koch Kellan Scholarship honors one outstanding graduate medical student committed to elevating the standard of eye care through social responsibility and a clinical, teaching, or research career in ophthalmology. A Paragon Gives initiative, the scholarship reinforces the fundamental mission of Paragon BioTeck to drive innovations to address unmet and underserved medical needs.

Download the 2018 Koch Kellan Scholarship application and guidelines at http://kochkellan.com/. Application materials will be accepted until January 16, 2018.

"The Koch Kellan Scholarship program celebrates the contributions of namesakes Drs. Koch and Kellan and fosters the future leaders in ophthalmology," said Patrick Witham, President & CEO of Paragon BioTeck. "Each year, we are astounded by the incredible pool of candidates and are honored that so many aim to cultivate an elevated standard of eye care. We are excited to welcome the next Koch Kellan Scholar to the Paragon family."

Applications will be reviewed by industry leaders Paul S. Koch, MD, and Robert E. Kellan, MD, along with additional members of the Scholarship Review Committee. The 2018 Scholar will formally be presented with the award at the 2018 American Society of Cataract and Refractive Surgery (ASCRS) annual meeting held April 13-17 in Washington, D.C.

The 2017 Koch Kellan Scholar, Xinxin Zhang, is a third-year student attending the University of North Carolina, Chapel Hill. Her passion for ophthalmology was confirmed during a research project dedicated to bringing diagnostic innovations to some of China's poorest provinces, where high rates of preventable blindness occur primarily due to lack of screening. She spent 2016 researching dry eye disease and leading UNC's student-run ophthalmology clinic.

About Paragon Gives and the Koch Kellan Scholarship:

Paragon Gives is a Paragon BioTeck, Inc., initiative that supports charities and organizations within the biotechnology and health care arena. The initiative also works with individuals and organizations that have made a positive impact on our customers, vendors, investors and industry as a whole.

The Koch Kellan Scholarship affirms the commitment of Paragon BioTeck to elevate the standard of eye care through addressing unmet and underserved medical needs and improving the quality of lives around the world. It was first awarded to Captain Edward Woodward of the University of South Florida Morsani College of Medicine, whose compelling personal connection to the field made him the ideal inaugural recipient. Learn more about our past scholars: http://kochkellan.com/scholars/.

About Paragon BioTeck, Inc.:

Paragon BioTeck, Inc. is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies. Paragon BioTeck's portfolio of products is designed to protect and preserve eyesight and deliver comfort to the eyes. Information: https://paragonbioteck.com/.

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MEDIA CONTACT:
Stefanie Henning
Paragon BioTeck, Inc.
888-424-1192
marketing@paragonbioteck.com

News from Paragon BioTeck, Inc.

Paragon BioTeck, Inc., a privately-held pharmaceutical and medical device company, today announced the call for the next Koch Kellan Scholar. The annual Koch Kellan Scholarship honors one outstanding graduate medical student committed to elevating the standard of eye care through social responsibility and a clinical, teaching, or research career in ophthalmology. A Paragon Gives initiative, the scholarship reinforces the fundamental mission of Paragon BioTeck to drive innovations to address unmet and underserved medical needs.

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Edmond Hooker, MD, Darrel Hicks, and Bruce Rippe Discuss Medical Mattress Contamination Issues on C.diff Spores and More, Aug. 1

TAMPA, Fla. /ScoopCloud/ -- C Diff Foundation's, "C. diff. Spores and More Global Broadcasting Network," is honored to announce Dr. Edmond Hooker, MD - Associate Professor of Health Services Administration at Xavier University, Darrel Hicks, a well-known hospital environment specialist and educator, and Bruce Rippe, CEO of Trinity Guardion, manufacturer of the Trinity Guardion Patient Protective Barrier, as our guest speakers on August 1, 2017 at 10 a.m. PT / 1 p.m. ET on www.cdiffradio.com.

These leading topic experts will be discussing Dr. Hooker's Clostridium difficile (C. diff.) research related to hospital beds and mattresses, the issues that prevent successful disinfection of soft mattress surfaces, the new regulatory landscape, and the proven solution to the problem. The data being shared will be beneficial to hospital nursing officers, infection preventionists, and environmental services professionals. Many healthcare professionals are unaware that hospital beds, which are the epicenter of patient care, can also be the epicenter of potentially life-threatening cross-contamination.

Trinity Guardion's patient protective microbarrier is the first and only launderable and reusable mattress cover system specifically for medical beds. It's designed to protect each patient and prolong the useful life of expensive high-tech hospital mattresses, by shielding the mattress and bed deck from every previous occupant's microbial biome. More importantly, it protects each patient from residual pathogenic organisms such as C. diff., which can cause serious illness and death, and may be present even if previous patients were not symptomatic.

If you miss the live broadcast, access the podcast in the living library and listen at your leisure www.cdiffradio.com.

About Trinity Guardion:
Founded in 2010 and based in Batesville, Indiana, Trinity Guardion manufactures the Trinity Guardion(R) Patient Protective Barrier, the only reusable and launderable cover system for hospital beds and bed decks that is specifically engineered to block and eliminate pathogens such as Clostridium difficile (C. diff.). The system delivers a validated cleaning and disinfection solution that is proven to reduce infection rates.

About the C Diff Foundation:
The C Diff Foundation, a 501(c)(3) non-profit, founded in 2012 by Nancy C. Caralla, a nurse who was diagnosed and treated for Clostridium difficile (C. diff.) infections. Through her own journey and the loss of their father to C. difficile infection involvement, Nancy recognized the need for greater awareness through education about research being conducted by the government, industry, and academia and better advocacy on behalf of patients, healthcare professionals, and researchers worldwide working to address the public health threat posed by this devastating infection.

For information please visit http://www.cdifffoundation.org/.

Media Coordinator
Denise Graham
denise@cdifffoundation.org

News from C Diff Foundation

C Diff Foundation's, "C. diff. Spores and More Global Broadcasting Network," is honored to announce Dr. Edmond Hooker, MD - Associate Professor of Health Services Administration at Xavier University, Darrel Hicks, a well-known hospital environment specialist and educator, and Bruce Rippe, CEO of Trinity Guardion, manufacturer of the Trinity Guardion Patient Protective Barrier, as our guest speakers on August 1, 2017.

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ScoopCloud Newswire

ChemDiv Selected by Arcus Biosciences as the Sole Chemistry Provider for its Discovery Screening Collection

SAN DIEGO, Calif. /ScoopCloud/ -- ChemDiv Inc., a fully integrated California-based CRO, announced today that Arcus Biosciences selected ChemDiv as the sole source of molecules for Arcus's growing HTS screening collection. This collaboration, which utilized Arcus's medicinal chemistry knowledge and ChemDiv's computational and synthetic chemistry expertise, has resulted in the selection of several hundred thousand structures from which Arcus expects to identify starting points for several of the discovery programs in its portfolio.

"A best-in-class drug always starts with a great lead, and our team has learned over the years, going back to our Tularik days, that ChemDiv's libraries have been carefully designed to increase the likelihood of identifying such great leads," said Juan Jaen, President and Co-Founder of Arcus Biosciences.

Jaen added: "Arcus currently has a number of small-molecule discovery programs targeted at the regulation of several biological pathways that appear to play important roles in the suppression of effector immune (T and NK) cells. Some of these programs are already fairly mature and will be in the clinic in short order; however, some of the earlier-stage projects will benefit immensely from having access to ChemDiv's compounds.

"ChemDiv's efficiency in producing high-quality, diverse, and medicinal chemistry-friendly compound collections, coupled with their ability to resupply compounds and build upon those initial hits with their Discovery Chemistry services makes ChemDiv a partner of choice for any organization, large or small, who is looking for a partner in small-molecule drug discovery."

"We are thrilled to have the opportunity to partner with Arcus Biosciences," commented Ron Demuth, General Manager of ChemDiv, Inc. "One of the most promising companies in the very competitive immune-oncology space and one of the few companies engaged in building a broad portfolio of internally designed small-molecule drugs for use in reversing the immunosuppressive tumor microenvironment; our priority is to help our partner by providing access to all the unique features of our expanding compound collection."

About ChemDiv:
ChemDiv is a recognized global leader in discovery chemistry with one of the industry's largest, most diverse, and most productive collections of over 1,600,000 individually crafted, lead-like, drug-like small molecules. Over the past 25 years the ChemDiv team has delivered hundreds of leads, drug candidates and new drug approvals in the areas of CNS, oncology, virology, inflammation, cardio and metabolic diseases to its pharma and biotech customers around the globe. ChemDiv's integrated drug discovery and evaluation platforms allow for an accelerated, cost-effective R&D process aimed at rapidly bringing a project from target ID to Phase 3 clinical candidate and beyond. More information: http://www.chemdiv.com/.

About Arcus Biosciences:
Arcus Biosciences is an exciting young company founded on a vision of creating new cancer therapeutics through the utilization of emerging insights in immunology. Arcus was formed in 2015 by a group of seasoned researchers from the biotechnology and pharmaceutical industries and is located in the San Francisco Bay area, in the heart of the world's largest biotechnology research hub. More information: https://www.arcusbio.com/

Media Contact:
Ronald Demuth
Senior VP, Corporate Development & General Manager
ChemDiv
+1(858)-794-4860x321
rdemuth@chemdiv.com

ChemDiv Inc., a fully integrated California-based CRO, announced today that Arcus Biosciences selected ChemDiv as the sole source of molecules for Arcus's growing HTS screening collection. This collaboration, which utilized Arcus's medicinal chemistry knowledge and ChemDiv's computational and synthetic chemistry expertise, has resulted in the selection of several hundred thousand structures from which Arcus expects to identify starting points for several of the discovery programs in its portfolio.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

ScoopCloud Newswire

Verify Smart Corporation Signs Letter of Intent to Acquire Equity Stake and Exclusive International Reseller Rights in Med-Con Technologies, LLC

FERNLEY, Nev. /ScoopCloud/ -- Verify Smart Corporation (OTC:VSMR / OTCMKTS:VSMR) a Global innovator in financial fraud prevention and digital distribution solutions announced today that it has signed a Letter of Intent to acquire an equity stake and exclusive international reseller rights in Med-Con Technologies, LLC for cash and stock.

Med-Con Technologies provides a patented solution (MedSked(TM)) for improved medication adherence. MedSked(TM) gives patients the ability to more effectively self-manage and keep track of their daily medication dosing. Med-Con's solutions are effectively assisting patients in over thirty two countries, and twenty four languages.

Med-Con has also developed MedCon Mobile Smart Label(TM) which is a mobile based patient adherence solution for the Pharmaceutical industry and is currently being tested by a major Pharmaceutical company with other pilots scheduled. The cloud based SaaS software manages the patient's medication dosing schedule via a mobile device while sending vital adherence data to the Pharmaceutical clinical trial teams for analysis via the MedCon Central(TM) data portal. Verify Smart and Med-Con believe this product is groundbreaking and a huge first to market play in the Pharmaceutical space.

Pharmaceutical Manufacturing Magazine said "Medication Adherence is arguably the largest problem in healthcare, it is estimated that medication non-adherence causes 30 - 50 percent of treatment failures and 125,000 deaths annually. The direct cost to healthcare is estimated as high as $289 billion annually. Pharmaceutical companies are motivated to increase adherence because higher compliance equates to better treatment effectiveness and overall better patient health...and of course, higher drug sales."

Tony Cinotti, President of Verify Smart said "Verify Smart will work closely with Med-Con Technologies to establish Verify Smart as the exclusive international reseller of MedSked and MedCon Mobile Smart Label for pharmaceutical companies, pharmacy chains and specialty pharmacy markets.

"Verify Smart will also, in parallel, build an additional adherence solution specifically for Retail Pharmacies. This will greatly increase Med-Con sales worldwide. Pharmacy customers taking prescription medications can now have the same benefits as Med-Con's corporate adherence solutions."

Anthony Londino, President of Med-Con Technologies commented "We are excited about working with Verify Smart to develop new products and broaden our reach into new markets and opportunities. Verify Smart's sales and marketing expertise, IT partners and extensive contacts in the retail pharmacy space will provide Med-Con with the additional resources to become the world leader in medication adherence and remote patient monitoring data."

About Verify Smart Corporation:
Verify Smart Corp is an international technology company that develops and markets innovative solutions for the global digital market. The company also licenses patented technology for the prevention of debit/credit card and electronic transaction fraud. The company is expanding into the growing digital and mobile sector and will market innovative solutions for pharmaceutical companies, consumer brands, educational institutions and the sports and entertainment industries.

Contact Info:
Verify Smart Corporation
Info@verifysmartcorp.com
775-575-5897
http://www.verifysmartcorp.com/

About Med-Con Technologies:
Med-Con Technologies LLC is a global provider of medication adherence solutions and services to the pharmaceutical market. Med-Con Technologies LLC has been helping some of the world's most prominent pharmaceutical companies to provide medication adherence support to their clinical trial and commercial patients. The company is expanding into the growing digital and mobile sector and has recently launched its MedSked Mobile Smart Label platform, a novel and innovative patient compliance solution.

Contact Info:
Med-Con Technologies LLC
http://www.medsked.com/
1-888-654-0856 ext. 125

REF: OTCMKTS:VSMR / OTC:VSMR / OTCBB:VSMR

Verify Smart Corporation (OTC:VSMR / OTCMKTS:VSMR) a Global innovator in financial fraud prevention and digital distribution solutions announced today that it has signed a Letter of Intent to acquire an equity stake and exclusive international reseller rights in Med-Con Technologies, LLC for cash and stock.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

ScoopCloud Newswire

EPIC Insurance adds Reba Mathew, Pharm.D., R.Ph to Employee Benefits Consulting Pharmacy Practice

HOUSTON, Texas /ScoopCloud/ -- EPIC Insurance Brokers and Consultants, a retail property, casualty insurance brokerage and employee benefits consultant, announced today that Reba Mathew Pharm.D., R.Ph has joined the firm's Employee Benefits Consulting Practice as Pharmacy Practice Director.

Dr. Mathew will be based in Houston, Texas and will report to Cliff Caldwell, Chief Operating Office of Ascende - a Division of EPIC.

Dr. Mathew completed her Managed Care Pharmacy Residency with one of the largest Medicare health plans. During her residency she worked on several pharmacy initiatives such as medication therapy management, pay for performance, and quality improvement.

In addition to residency, Dr. Mathew has worked as a clinical pharmacist in both the hospital and retail setting. Her significant clinical experience led her to the pharmacy consulting practice for two of the world's largest brokerage services, managing nearly $250 million annually in pharmacy benefits.

Dr. Mathew was able to achieve significant clinical goals for her clients, including improvement in generic dispensing rates and medication adherence, implementation of customized and standard utilization management programs and formularies, and reduction in total pharmacy spend.

Said Cliff Caldwell, "We are pleased and excited to have Reba join Robin Rankin R. Ph in leading our Pharmacy Practice team and the Ascendent Pharmacy Coalition. Her knowledge, depth of experience and strong, client-focused consulting skills deepen and strengthen the resources and services available to EPIC clients across the country."

Dr. Reba Mathew can be reached at:
Ascende - a Division of EPIC
Office: 832-476-8454
Mobile: 713-515-8058
reba.mathew@epicbrokers.com
rmathew@ascende.com

About the Ascendent(R) Pharmacy Coalition:

Launched in 2002, the Ascendent(R) Pharmacy Coalition brings the power of a purchasing coalition to mid-market clients looking for a more effective means of delivering transparent pharmacy pricing and discounted rates. Participants in the coalition realized over $100 Million dollars in savings in 2016.

About EPIC:

EPIC is a unique and innovative retail property and casualty and employee benefits insurance brokerage and consulting firm. EPIC has created a values-based, client-focused culture that attracts and retains top talent, fosters employee satisfaction and loyalty and sustains a high level of customer service excellence. EPIC team members have consistently recognized their company as a "Best Place to Work" in multiple regions and as a "Best Place to Work in the Insurance Industry" nationally.

EPIC now has more than 1,000 team members operating from offices across the U.S., providing Property Casualty, Employee Benefits, Specialty Programs and Private Client solutions to more than 20,000 clients.

With roughly $280 million in run rate revenues, EPIC ranks among the top 20 retail insurance brokers in the United States. Backed by the Carlyle Group, the company continues to expand organically and through strategic acquisitions across the country.

For additional information, please visit http://www.epicbrokers.com/.

MEDIA CONTACTS:
Dave Hock
650-295-4608
dave.hock@epicbrokers.com

Nicole Conley
408-295-4309 x104
nicole.conley@taniscomm.com

*PHOTO for media: Send2Press.com/mediaboom/17-0516s2p-Reba-Mathew-300dpi.jpg

EPIC Insurance Brokers and Consultants, a retail property, casualty insurance brokerage and employee benefits consultant, announced today that Reba Mathew Pharm.D., R.Ph has joined the firm's Employee Benefits Consulting Practice as Pharmacy Practice Director.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

Medical Experts Unite Regarding Health Benefits of Testosterone Therapy in Women

IRVING, Texas /ScoopCloud/ -- BioTE(R) Medical announces a forum of medical experts gathering before the Age Management Medicine Group (AMMG) to form consensus on testosterone therapy in women.

The Age Management Medicine Group (AMMG) conference runs April 27-30, 2017 in Orlando, Florida. Learn more: https://www.agemed.org/.

Nine experts, from across the United States, spanning a variety of medical disciplines and specialties, will present data then defend and vet topics related to testosterone therapy in women.

They will form a consensus and present their position at the next AMMG Conference in November in Tucson, Arizona. Their work will be submitted to medical journals for publication with the goal of gaining widespread support for the use of testosterone therapy in women.

Testosterone has shown to be one of the most cardio-protective hormones and the consensus group will make recommendations that could significantly improve healthcare and reduce heart disease in women - the number one cause of death in women and men in the United States.

Most of the research commentary on BHRT focuses on the effects of testosterone therapy in men. Yet, the data is there to support the health advantages in women. Women derive many of the same benefits from testosterone therapy as men regarding muscle mass, strength, and libido. Additionally, BHRT is protective to the brain, breast, bones, and heart. It helps reverse the annoying symptoms of declining hormones like fatigue, low energy, difficulty inability to lose weight, and irritability and it can increase bone density and help prevent age-related illnesses like osteoporosis and Alzheimer's.

Click on the link below to hear Founder and CEO of BioTE(R) Medical, Gary S. Donovitz, M.D. share the truth about hormone therapy and the critical need for this consensus.

Video (YouTube): https://youtu.be/kLecmEk7Vtg

For information on the AMMG Conference visit https://www.agemed.org/.

BioTE(R) Medical was founded by physicians for physicians and is committed to excellence in educating doctors and clients about the health benefits of bioidentical hormone pellet therapy. BioTE(R) is headquartered in Irving, Texas and has thousands of certified medical practitioners nationwide. See more about BioTE at http://www.BioTEmedical.com/.

*PHOTO for media: Send2Press.com/mediaboom/17-0419s2p-Gary-Donovitz-300dpi.jpg

*Photo Caption: BioTE(R) Medical Founder and CEO, Gary S. Donovitz M.D.

BioTE(R) Medical announces a forum of medical experts gathering before the Age Management Medicine Group (AMMG) to form consensus on testosterone therapy in women. The AMMG conference runs April 27-30, 2017 in Orlando, Florida.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

ScoopCloud Newswire

Delta Care Rx Announces Patrick White, MD, Inaugural Recipient of Delta Distinguished Scholar Award

PITTSBURGH, Pa. /ScoopCloud/ -- Delta Care Rx today announced the first-ever recipient of the Delta Distinguished Scholar award. Patrick White, MD, HMDC, FACP, FAAHPM, chief medical officer of BJC Hospice, St. Louis, http://www.bjchospice.org/, and assistant professor of medicine at Washington University, has received an initial $25,000 research grant, with a $500,000 lifetime potential, for study into the comparative and cost effectiveness of pharmaceuticals.

"Even if we can't cure, there are ways to relieve symptoms," says White, whose choice of hospice medicine was influenced by his experience at age 7, when he visited patients with cystic fibrosis with his father, a pulmonologist.

"Improving a cough or alleviating shortness of breath meant the world to those patients and their families," he says. "Now, through the research initiated by this grant, my team and I have a tremendous opportunity to reduce suffering and identify those most likely to benefit from particular drug therapies at end of life."

Delta Care Rx, www.deltacarerx.com, is a leading pharmaceutical innovator in the field of hospice medicine, offering its clients unparalleled transparency in the effectiveness and cost of medications. With an average of 1.5 million patients receiving hospice care annually in the U.S., the potential impact of White's research on symptom management and pain control has widespread implications.

White is distinguished by his "commitment to take hospice and palliative medicine to a higher level of extreme, patient-focused care," according to Delta Care Rx CEO Mary Mihalyo, PharmD, BCPS, CDE.

Mihalyo is a widely respected pioneer in the specialty of hospice pharmacy.

"In hospice and palliative medicine, there is a lack of evidence identifying the true pharmaco-economic nature of medications we use daily," says Mihalyo. "The hospice profession needs physicians who are also researchers."

To date, pharmaceutical research in hospice medicine is limited. Hospice patients are excluded from most clinical trials. This exclusion makes it difficult to determine which drug therapies are effective for hospice patients, and which are not. Too often, hospice clinicians must make choices based on affordability, not on efficacy.

"Some commonly prescribed medications actually reduce quality of life for hospice patients and offer no benefit toward survival," White says.

The award announcement follows closely that of last week's selection of White to serve on the Missouri Governor's interdisciplinary council on palliative care and quality of life. He currently serves as chair of the palliative care committee of the Missouri Hospice and Palliative Care Association, and sits the national Hospice Medical Director's Leadership Council of the American Academy of Hospice and Palliative Medicine.

"Patrick White exemplifies the physician-researcher model and has a demonstrated interest in cost effective medication use," says Mihalyo.

In hospice settings, clinicians need the ability to distinguish between medications that are believed to work but may not, and those which actually work, but may be underutilized. The specific medications studied under the auspices of the grant remain undisclosed.

"A talented researcher like Patrick White may be able to prove that newer medications are equally cost effective to those used historically," she says. "That would be very valuable information."

Through professional practice, White has experienced firsthand the costs associated with a lack of evidence for pharmaceutical use. Also, he offers demonstrated ability to build collegial relationships across the continuum of care to conduct the research needed.

"Identifying evidence through research allows those of us within the profession to develop patient-specific ways to identify the most appropriate intervention - which is not always the least expensive medication on the market," says Mihalyo.

The Delta Distinguished Scholars Program selects leading physician-researchers with expertise in hospice medicine for career development funding to offset direct research costs. Preference is given to early career investigators, like White, who have the potential to significantly impact the field.

"I am especially grateful this award came from Delta Care Rx," says White. "They are an integral part of the effort to advance the cause of quality patient-centered care."

The Delta Care Rx Hospice Taper(c) transparent and pass-through drug purchasing model should be the "gold standard," he says. The model assures that the amount a hospice pays for medication is always equal to the amount the dispensing pharmacist is reimbursed for filling an order.

In contrast, many hospice pharmacy benefit managers charge the hospice one amount then reimburse the dispensing pharmacist at a much lesser amount. The result is higher daily costs of care.

White hopes his team's research "will result in improved patient outcomes with a lower cost of care per day."

"When hospices are able to afford medications they couldn't previously because of price, patients get the interventions they deserve," says Drew Mihalyo, PharmD, Delta Care Rx founder, president, and COO. "As Dr. White considered the concept of enhanced access to medications, it set the framework for future research, which Delta Care embraced."

The Delta Scholar Award is by invitation only and will not occur annually. Successful applicants demonstrate a strong research background in comparative effectiveness or cost effectiveness research, outstanding leadership skills, and a proven commitment to advancing the field of hospice research. Physician-researchers may request an invitation to apply at http://www.deltacarerx.com/delta-campus/research.

About Delta Care:

Delta Care, http://www.deltacarerx.com, transforms and improves the hospice pharmacy industry through business transparency, innovation, extreme customer service, and the maintenance of vital community-pharmacy relationships. As a pharmacist owned, privately held provider, Delta Care sets the industry benchmark for pharmacy benefit management, on-demand pharmacist services, and hospice tailored electronic prescribing. Additionally, Delta Care offers tools and technologies to simplify essential workflow and ordering processes within hospice settings.

*PHOTO for media: Send2Press.com/mediaboom/17-0418s2p-Patrick-White-300dpi.jpg
*LOGO: Send2Press.com/mediaboom/17-0418s2p-delta-care-300dpi.jpg

Delta Care Rx today announced the first-ever recipient of the Delta Distinguished Scholar award. Patrick White, MD, HMDC, FACP, FAAHPM, chief medical officer of BJC Hospice, St. Louis, and assistant professor of medicine at Washington University, has received an initial $25,000 research grant, with a $500,000 lifetime potential, for study into the comparative and cost effectiveness of pharmaceuticals.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

ScoopCloud Newswire

Trump’s wrong attack on Opioid Epidemic

CORTE MADERA, Calif. /ScoopCloud/ -- Dr. Don Harte, chiropractic activist, says Trump's new panel, headed by Chris Christie, to deal with the opioid epidemic, is "philosophically and scientifically dead wrong."

Dr. Harte declares, "The reason for this epidemic is clear. Orthopedists and other doctors freely prescribe Oxycontin, Fentanyl, Soma and other opioid drugs, get their patients addicted, then cut them off. These patients end up seeking heroin on the street. It all begins in the doctor's office. It ends in pain, life disruption and, often, death."

"It begins with sciatica, arthritis, carpal tunnel syndrome, or some sports injury," Dr. Harte says. "Modern orthopedic medicine can do nothing to fix these things. This opioid epidemic is emblematic of the failure of Medicine."

Dr. Harte continues, "While they can't get you better, orthopedists can and do make conditions, and pain, worse, in two ways. Cortisone shots damage already-damaged (by anti-inflammatories) joint surfaces. Spinal surgery has such a bad record that they have a name for their failures... 'Failed back surgery syndrome.' And when joint replacements aren't right, it's disastrous!" He charges, "This is irresponsible science; it is irresponsible doctoring."

"There is no hope," says Dr. Harte, "in pain management. It fixes nothing, while causing constipation and sleep problems, lung and heart damage, as well as addiction. To empower the government to provide more and better rehab for opioid addicts, created by medical care, is not the answer! Such a safety net will likely lead to a bigger epidemic."

Dr. Harte's answer to this crisis? "The only answer to the current life-destroying opioid epidemic is to point the finger at orthopedic medicine, and lead the way to safe and effective chiropractic care, on a widespread basis. It is high time that people reject what does not work, and seek what does." He concludes, "Chiropractic works. It corrects cause, with zero risk for addiction."

Dr. Don Harte, former medical student, is a traditional chiropractor, serving Marin and the Greater Bay Area since 1981. He is an activist in the struggle for free speech for chiropractors. Dr. Harte was named 2006 "Chiropractor of the Year" by the World Chiropractic Alliance (WCA). He has served on the Boards of the WCA and the Council on Chiropractic Practice. His articles have been published in OMNI magazine, San Francisco Chronicle, Chiropractic Journal and Journal of the California Chiropractic Association.

The Harte of Chiropractic, Prof. Corp. - http://www.chirodrharte.com/

Media Contact:
Dr. Harte
The Harte of Chiropractic,
415-847-9678

Dr. Don Harte, chiropractic activist, says Trump's new panel, headed by Chris Christie, to deal with the opioid epidemic, is "philosophically and scientifically dead wrong." Dr. Harte declares, "The reason for this epidemic is clear. Orthopedists and other doctors freely prescribe Oxycontin, Fentanyl, Soma and other opioid drugs, get their patients addicted."

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

ScoopCloud Newswire

Ruling Affirms Patent Claim for Paragon BioTeck’s R-Phenylephrine Hydrochloride Formulation

PORTLAND, Ore., /ScoopCloud/ -- Paragon BioTeck, Inc. (Paragon), announces a monumental ruling handed down by the United States Patent and Trademark Office affirming claims made by Paragon in the patent for its R-phenylephrine hydrochloride formulation. Paragon is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies.

In late 2015, Altaire Pharmaceuticals, Inc., sought to invalidate Paragon's patent that claims a method of maintaining purity of the formulation. In only the fourth written decision by the Patent Trial and Appeals Board, the ruling affirms that the petition by Altaire Pharmaceuticals was without merit.

"While our belief in the strength of our patent was never in doubt, this is a tremendous win for Paragon BioTeck. This continues to reaffirm our belief and company mission behind the science and products we develop," said Patrick Witham, President & CEO.

Paragon is strongly dedicated to addressing unmet and underserved medical needs through product development that is based on cutting-edge science. Since its inception, Paragon has sought to partner with leading scientists and thinkers to drive innovations that advance patient care and improve the quality of lives around the world.

The patent ruling both reinforces the strong science underlying the formulation of Paragon's Phenylephrine Hydrochloride Ophthalmic Solution and substantiates the operational philosophy of the company.

Phenylephrine hydrochloride is widely used by eye care professionals to attain mydriasis (dilation of the pupil) for conducting an ocular examination. It is an indispensable tool for the early detection, diagnosis and treatment of serious eye diseases and is vital in managing ocular health.

About Phenylephrine Hydrochloride Ophthalmic Solution:

Phenylephrine Hydrochloride Ophthalmic Solution, USP 2.5% and 10%, is an alpha-1 adrenergic receptor agonist used for dilation of the pupil due to its vasoconstrictor and mydriatic action. Phenylephrine possesses predominantly adrenergic effects. In the eye, phenylephrine acts locally as a potent vasoconstrictor and mydriatic by constricting ophthalmic blood vessels and the radial muscle of the iris.

Phenylephrine Hydrochloride Ophthalmic Solution Important Safety Information:

Phenylephrine Hydrochloride Ophthalmic Solution, USP 10%, is contraindicated in patients with hypertension or thyrotoxicosis, as well as in pediatric patients under the age of one due to the increased risk of systemic toxicity. Phenylephrine Hydrochloride Ophthalmic Solution, USP 2.5%, should not be used in these patients. Phenylephrine Hydrochloride Ophthalmic Solution, USP 10% and 2.5% is for topical ophthalmic use only, and not for injection.

Serious cardiovascular reactions, including ventricular arrhythmias and myocardial infarctions, some fatal, and significant elevations in blood pressure have been reported. Caution is advised in pediatric patients less than five years of age and in patients with elevated blood pressure, cardiovascular disease or hyperthyroidism. Blood pressure should be monitored in patients with cardiovascular or endocrine disease. Rebound miosis has been reported one day after instillation.

Ocular adverse reactions include eye pain and stinging on instillation, temporary blurred vision and photophobia. Cardiovascular adverse reactions include increase in blood pressure, syncope, myocardial infarction, tachycardia, arrhythmia and subarachnoid hemorrhage.

About Paragon BioTeck, Inc.:

Paragon BioTeck, Inc. ( https://paragonbioteck.com ), is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies. Paragon's portfolio of products is designed to protect and preserve eyesight and deliver comfort to the eyes. These products include the Comfortear(r) Lacrisolve(tm) 180 Absorbable Punctum Plug, Comfortear(r) Punctum Plug, the preservative-free ilast(r) range of products and their FDA-approved Phenylephrine Hydrochloride Ophthalmic Solution, USP 2.5% and 10%.

Media Contact:
Allison Potter Howell
Senior Account Director
Pascale Communications, LLC
412-228-1678
allison@pascalecommunications.com

Paragon BioTeck, Inc. announces a monumental ruling handed down by the United States Patent and Trademark Office (USPTO) affirming claims made by Paragon in the patent for its R-phenylephrine hydrochloride formulation. Paragon is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies.

This version of news story was published on ScoopCloud™ (ScoopCloud.com) - part of the Neotrope® News Network - all rights reserved.

BioTE Medical Poised to Change Healthcare as it Expands into Georgia

bioidentical hormone replacement

ATLANTA, Ga., May 11, 2016 (SEND2PRESS NEWSWIRE) -- BioTE(R) Medical, a leader in bioidentical hormone replacement therapy (BHRT), is expanding its nationwide network of certified physicians into the Atlanta, Georgia market this month.

BioTE(R) Medical has experienced rapid growth in just a few short years due to physicians and patients seeking natural alternatives to synthetic hormone products to reverse the symptoms that decreasing hormone levels can cause. BioTE(R) uses cardio-activated pellets about the size of a grain of rice which are inserted just below the surface of the skin. This allows a patient to receive hormones consistently in the same way the body releases them naturally for up to six months. This beats other methods that must be applied weekly and sometimes daily rendering inconsistent results.

National health and fitness celebrity Larry North states, "The fact that I can live better with optimized hormones with only two treatments a year has changed the way I actually live my life. I think about all the hours I spent receiving weekly shots.... I will never get all that time back that I could have spent with my family."

BioTE(R) founder and president, Gary Donovitz, M.D., says, "At BioTE, we offer a natural way for patients to experience the benefits of BHRT using the BioTE method. We work to optimize hormone levels unique to each individual. This helps maximize the benefits a patient can receive. Thousands of our patients across the United States experience life-changing results monthly. We are committed to changing healthcare by allowing patients to take control of the quality of their lives while protecting their health. It is time for us to expand our 1200+ provider network into Georgia to meet the demand we are seeing across the nation."

The benefits of BHRT are far from new. Almost 80 years of data support that BHRT can prevent of age-related illnesses in men and women. BHRT can ease symptoms that often accompany declining hormone levels and help patients experience increased mental clarity, a greater ability to lose stubborn pounds, improved muscle strength, better sleep, fewer mood swings, and more energy. Also, optimized hormones help protect the brain, bones, breasts, and heart and can increase bone mass up to 8.3% per year.

Celebrity, author, and health advocate, Suzanne Somers, is a firm believer in the benefits of BHRT. In her conversation with Dr. Donovitz, she reveals how hormone therapy is the best thing she has ever done for herself and her marriage (VIDEO): https://youtu.be/udAoT9sJTgs .

BioTE(R) Medical's network of physicians are trained by world-renowned doctors. BioTE's panel of trainers and speakers comprises the most highly qualified, most knowledgeable experts in hormone optimization in the world. Once certified, physicians have on-going access to BioTE(R) Medical's experts and receive continuing education opportunities to stay up-to-date on the most current BHRT information available.

To receive your free copy of Dr. Donovitz's best-selling book, "Age Healthier, Live Happier," pre-register now for an upcoming BioTE(R) Medical seminar in the Atlanta area*: http://www.biotemedical.com/signup .

Learn more about BioTE(R) and the benefits of BHRT at http://www.BioTEmedical.com .

*Free copies available to the first 100 pre-registrants. Must attend the seminar to receive Dr. Donovitz's book.

BioTE(R) Medical was founded by physicians for physicians and is committed to excellence in educating doctors and clients about the health benefits of bioidentical hormone pellet therapy. BioTE(R) is headquartered in Irving, Texas and has over one thousand certified medical practitioners nationwide.

For media questions on BioTE(R) Medical and more video clips, or to set up an interview with Gary Donovitz, M.D., please contact:
Christian Sly, President or
Sarah Harron, Production Manager
Omni Visual Media (OVM)
P: 214-212-8606
christian@omnivisualmedia.com

Twitter: @BioTEMedical

*PHOTO for media: Send2Press.com/mediaboom/16-0511-biote-med-300dpi.jpg

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/biote-medical-poised-to-change-healthcare-as-it-expands-into-georgia-2016-0511-02.shtml.

NEWS SOURCE BioTE Medical :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2016 Send2Press® Newswire, a service of Neotrope®.

W&L Hopes Faster FDA Publication of Potential Risk Signals for SGLT2 Inhibitors: Newest – Stroke, Thromboembolic Events, Acute Kidney Injury

consumer protection law

NEW YORK, N.Y., April 1, 2016 (SEND2PRESS NEWSWIRE) -- Weitz & Luxenberg, P.C., said today it hopes potentially fatal side effects associated with SGLT2 inhibitor drugs will be reported to consumers faster, since people taking these next-generation diabetes medications deserve to be notified of the health dangers shortly after they have been reported to the U.S. Food and Drug Administration (FDA).

Unfortunately, the most recent report of serious potential side effect risks were not announced by the FDA this year until after a significant delay, the nationally known law firm said.

In lists of these medications and their side effects published this year, the FDA stated it has now identified potential new signals of serious risk for people taking SGLT2 inhibitors, including strokes, thromboembolic events and acute kidney injury, Weitz & Luxenberg pointed out.

The potential risk of strokes and thromboembolic events was detected during the second quarter of 2015 and should have been published on the FDA's website by the end of the third quarter of last year. Weitz & Luxenberg has learned, however, that this potential safety signal was not posted on the FDA's website until February of this year, four months overdue.

The potential risk for acute kidney injury had been determined by the FDA based on data received from consumers and healthcare providers between October and December of last year, said Weitz & Luxenberg.

Concerns with SGLT2 Inhibitors Identified:

There are currently seven SGLT2 inhibitor drugs. All of them were listed under the potential signals of serious risk for stroke, thromboembolic events and acute kidney injury. The FDA became aware of these potential serious risks through its Adverse Event Reporting System (FAERS), according to Weitz & Luxenberg.

The law firm said the seven SGLT2 inhibitor drug brands listed in the two FDA lists of potential signals of serious risks are:
* Invokana (canagliflozin)
* Invokamet (canagliflozin/metformin HCl)
* Farxiga (dapagliflozin)
* Glyxambi (empagliflozin/linagliptin)
* Jardiance (empagliflozin)
* Synjardy (empagliflozin/metformin HCl)
* Xigduo XR (dapagliflozin/metformin HCl).

SGLT2 (sodium-glucose cotransporter-2) inhibitors are prescription medicines approved by the FDA to treat adult type 2 diabetes mellitus when combined with diet and exercise, said Weitz & Luxenberg.

SGLT2 inhibitors are prescribed in an attempt to lower blood sugar levels.

A growing body of scientific literature and adverse event reports made to regulatory bodies around the world, including the FDA, have linked SGLT2 inhibitors to a spectrum of serious adverse health consequences, the law firm said.

Lawsuits Commenced:

In 2015, Weitz & Luxenberg launched an investigation of those adverse health consequences. The firm said its findings convinced it to begin accepting cases from consumers injured by SGLT2 inhibitors.

The firm has filed five cases on behalf of individuals who suffered from diabetic ketoacidosis, who then went on to suffer one of the following devastating events: coma, kidney injuries, and infection leading to necrotizing fasciitis. Those cases are pending in the Court of Common Pleas of Philadelphia County.

Individuals Who Suffered Harm from SGLT2 Inhibitors Deserve Help:

Weitz & Luxenberg said delays in government reporting of newly-identified potential SGLT2 inhibitor health risks have not slowed the effort to bring the drugs' manufacturers to justice.

Still, attorneys within the firm said it would be beneficial to the public were FAERS reports made available sooner.

"By the time consumers find out there is a new pattern of problems being reported to the FDA with SGLT2 inhibitors, it may be too late, as many of them will by then have already suffered a devastating medical event," said attorney Ellen Relkin, who is leading the Weitz & Luxenberg SGLT2 inhibitors investigation.

"The FDA should consider ways to improve the processes by which it acquires and analyzes adverse event data, and also the processes by which it produces and readies FAERS reports," Relkin added.

Relkin said her firm is interested in hearing from adult patients who took an SGLT2 inhibitor and then experienced diabetic ketoacidosis requiring hospitalization, renal failure or acute kidney injury requiring hospitalization, stroke or other thromboembolic events, such as blood clots in the legs (deep vein thrombosis or "DVT") or lungs (pulmonary embolism or "PE").

She said Weitz & Luxenberg also is interested in talking to individuals who took SGLT2 inhibitors and were hospitalized after suffering urinary tract infections resulting in blood infections (urosepsis) or kidney infections (pyelonephritis).

Relkin said individuals harmed in any of these ways may be entitled to reimbursement for the cost of hospitalization and any related medical care, in addition to other expenses, plus lost wages and more.

About Weitz & Luxenberg

Weitz & Luxenberg P.C. is among the nation's leading and most readily recognized personal injury and consumer protection law firms. Weitz & Luxenberg's numerous litigation areas include: mesothelioma, defective medicine and devices, environmental pollutants, products liability, consumer protection, accidents, personal injury, and medical malpractice. Victims of consumer fraud are invited to rely on Weitz & Luxenberg's more than 25 years of experience handling such cases. You can contact the firm's Client Relations department at 800-476-6070 or at info@weitzlux.com.

More information: http://www.weitzlux.com/.

Twitter: @WeitzLuxenberg

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/wl-hopes-faster-fda-publication-potential-risk-signals-sglt2-inhibitors-newest-stroke-thromboembolic-events-acute-kidney-injury-2016-0401-02.shtml.

NEWS SOURCE Weitz and Luxenberg P.C. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2016 Send2Press® Newswire, a service of Neotrope®.

Paragon BioTeck Receives EN ISO 13485:2012 Certification

medical devices

PORTLAND, Ore., March 29, 2016 (SEND2PRESS NEWSWIRE) -- Paragon BioTeck, Inc., a privately held pharmaceutical and medical device company, announced today that it has received EN ISO 13485:2012 certification, signifying the company's successful implementation of an effective quality management system.

The EN ISO 13485:2012 certification was awarded by the International Organization for Standardization, the world's largest developer and publisher of global quality and safety standards. This certification outlines specific requirements to establish and execute a structured quality management system for medical devices across all areas, from development to supply.

"Achieving this certification is an important milestone for Paragon BioTeck," said Lauren M-C Bluett, Director of Quality Assurance. "We have implemented a robust quality management system that conforms to ISO's global standards, demonstrating our commitment to excellence in product and operations through continuous improvement and quality by design."

Receipt of this certification paves the way for continued advancement of quality systems that meet world-class standards and maintain a central focus on patient safety and care.

About Paragon BioTeck, Inc.:

Paragon BioTeck, Inc., is a privately held pharmaceutical and medical device company specializing in the development and commercialization of ophthalmic pharmaceuticals, devices and therapies. Paragon BioTeck's portfolio of products is designed to protect and preserve eyesight and deliver comfort to the eyes.

These products include the Comfortear(R) Lacrisolve(TM) 180 Absorbable Punctum Plug, Comfortear(R) Punctum Plug, EqualEyes(R) Ocular Lubricant, the preservative-free ilast(R) range of products and their FDA-approved Phenylephrine Hydrochloride Ophthalmic Solution USP, available in 2.5% and 10%.

For more information about Paragon BioTeck and its products, please visit http://www.paragonbioteck.com/.

Join the conversation on Facebook ( https://www.facebook.com/ParagonBioTeck/ ) and Twitter: @ParagonBioTeck.

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MEDIA CONTACT:
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(484) 620-6167

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NEWS SOURCE Paragon BioTeck, Inc. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2016 Send2Press® Newswire, a service of Neotrope®.

eAgile Announces the Production Launch of the eSeal RFID Solution for Sealed Caps and Closures

eSeal RFID Solution

GRAND RAPIDS, Mich. and ZURICH, Switzerland, Jan. 26, 2016 (SEND2PRESS NEWSWIRE) -- eAgile Inc. (eAgile.com/eSeal), a global leader in radio frequency identification (RFID) technologies, announces the successful high-volume production launch of the eSeal heat induction solution. eSeal is the first turnkey solution engineered to integrate the benefits of RFID into the billions of caps and closures consumed by the over-the-counter pharmaceutical, nutraceutical, cosmetic and chemical manufacturers.

The production launch of eSeal follows pilot runs at multiple facilities where millions of RFID-enabled closures were introduced to the supply chain. "In today's world, consumers are demanding safety, especially as it relates to healthcare products. Similarly, brand owners and everyone in the supply chain want to provide the safest products possible. eSeal has proven to establish an unprecedented level of security and authenticity in one easy-to-implement solution," stated Gary Burns, CEO of eAgile. "Having deployed eSeal at a significant scale, a full array of supply-chain management benefits were provided from the visibility gained by item level tagging. In addition, we achieved the client's goals of anti-diversion and enhanced security."

Working as a stand-alone or in conjunction with current security technologies, eSeal integrates a uniquely encoded RFID inlay between the closure and the seal of the product. The final deliverable is a complete cap and seal which is easily substituted into current production equipment. eAgile's Integration services complete the system by installing RFID hardware and middleware software to provide relevant data to current ERP or data management applications at strategic locations throughout the supply chain.

"Customers are amazed at how quickly eAgile is able to integrate the eSeal solution within their facilities. The benefits are delivered and the business case is validated almost immediately. eAgile's tagline is 'RFID Made Easy' and we use this to guide our solutions development as well as our on-site integration strategy," explained Peter Phaneuf, President of eAgile. "eSeal does more than protect against counterfeiting and product diversion: it provides our clients the ability to refocus efforts back onto core business activities."

eSeal is proving invaluable to stakeholders at all levels and feedback is overwhelmingly positive. Real-time information gathered by the integrated system is used for anti-diversion applications, supply-chain management and product availability within distribution centers and retailers. eAgile is now focusing on enhancing brand interaction opportunities by linking consumers and their NFC-enabled smartphones to authentication-, expiration-, and dosing-information along with re-purchase and promotional opportunities.

eSeal is the latest technology release to leverage eAgile's intellectual property portfolio which includes eSync - a data management package controlling the synchronization of RFID encoding to printed barcodes and serialization at a market-leading 99.99975% accuracy - and over 20 other issued U.S. and international patents and filings. This commitment has led to industry-recognized milestones including one of the world's largest on-going RFID-based asset tracking programs.

About eAgile Inc.:

eAgile, headquartered in Grand Rapids, Mich., sets the standard in RFID solutions by providing high-quality, cost-effective auto-identification products finely tuned to customer needs. eAgile has one of the broadest ISO 9001:2008 certifications covering tag production, data management software and the building of complete RFID infrastructures. Learn more about eSeal and view a product demonstration video at http://www.eAgile.com/eSeal/.

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To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/eagile-announces-the-production-launch-of-the-eseal-rfid-solution-for-sealed-caps-and-closures-2016-0126-02.shtml.

NEWS SOURCE eAgile Inc. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2016 Send2Press® Newswire, a service of Neotrope®.

BioTE Medical Study Showing Promising Results for Military Veterans Diagnosed with PTSD and TBI

Medical Combat Trauma

IRVING, Texas, Dec. 30, 2015 (SEND2PRESS NEWSWIRE) -- A current BioTE(R) Medical Combat Trauma Treatment Study (in conjunction with the Veterans Advocacy Center (VAC)) is showing promising results in helping veterans suffering from Post-Traumatic Stress Disorder (PTSD) and Traumatic Brain Injury (TBI).

Founder of BioTE(R) Medical, Gary Donovitz, M.D., explains it this way: "Many veterans return from combat with PTSD and TBI. They have hormone imbalances that start in the pituitary gland. We are optimizing their hormones to help relieve their symptoms naturally. We do this by using bioidentical hormones instead of conventional prescription medication. This can improve the quality of their lives."

This study is FREE and available in 40 different states. It is open to veterans who have been discharged, are retired, or are still serving. It includes treatment and lab work (up to $2,000 in value). With such promising results, the program is still looking for qualified participants through the end of 2015.

If you or anyone you know might be interested in this study, please contact Mandy Cotten, DNP, APRN, FNP-C at mandy.cotten@BioTEmedical.com or go to http://www.biotemedical.com/ .

You can also contact Dr. Gary Donovitz online to schedule a speaking appearance or request more information.

Here is what two veterans have to say about their treatment so far: http://www.biotemedical.com/combat-trauma-tbi-and-ptsd-treatment-study.html .

About Dr. Gary Donovitz:

Gary Donovitz MD is the founder of BioTE(R) Medical and a renowned gynecologist in the Arlington, Texas area. Dr. Donovitz is an international instructor of the procedure and long-time proponent of Bio Identical Hormone Therapy (BHRT) who treats both men and women. In 2007, Dr. Donovitz received advanced training in BHRT and has trained more than 1,000 practitioners nationwide. He is Board Certified and is a Fellow in the American College of Obstetrics and Gynecology. To learn more about Dr. Gary Donovitz, visit his website: http://www.garydonovitzmd.com/ .

VIDEO (YouTube): https://youtu.be/vF7uDVsFIw8 .

Twitter: @BioTEMedical #PTSD #HormoneBalance #BioTE

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/biote-medical-study-showing-promising-results-for-military-veterans-diagnosed-with-ptsd-and-tbi-2015-1230-02.shtml.

NEWS SOURCE BioTE Medical :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.

Weitz and Luxenberg Adds Serious Urinary Tract Infections to SGLT2 Inhibitor Injuries Probe

consumer protection law

NEW YORK, N.Y., Dec. 7, 2015 (SEND2PRESS NEWSWIRE) -- Weitz & Luxenberg, P.C., today announced that the firm has expanded the scope of its investigation into SGLT2 inhibitor drug injuries. SGLT2 inhibitor drugs include Invokana and others listed below. This move will allow the nationally known mass tort law and personal injury firm to focus on cases where people taking SGLT2 inhibitors were hospitalized after developing urosepsis (serious infection of the blood) or pyelonephritis (infection of the kidneys) from SGLT2 inhibitor-associated urinary tract infections (UTIs).

Weitz & Luxenberg's decision to add serious urinary tract infections resulting in urosepsis or pyelonephritis to its probe came after the U.S. Food and Drug Administration (FDA) announced manufacturers of SGLT2 inhibitors would be required to include a warning about the risks of serious UTIs associated with this class of medication, the law firm said.

The FDA conveyed this new requirement in an updated Safety Communication issued on Dec. 4, 2015, said attorney Ellen Relkin, who is leading the Weitz & Luxenberg defective drug and medical devices's SGLT2 inhibitor investigation.

In the same Safety Communication, the FDA said SGLT2 inhibitor labels must also contain warnings about the risks of another serious complication that can occur - diabetic ketoacidosis.

Ketoacidosis is a serious condition in which blood acids called ketones are produced in high concentrations. The condition can be fatal if it goes untreated.

The FDA explained that the new requirement for SGLT2 inhibitor labels was prompted by reports appearing in the FDA Adverse Event Reporting System (FAERS). These reports linked SGLT2 inhibitors with many cases of patients developing ketoacidosis and SGLT2 inhibitor-associated UTIs to cases of patients developing serious urosepsis or pyelonephritis, resulting in hospitalizations.

Urosepsis is a potentially life-threatening blood infection, while pyelonephritis is a serious infection of the kidneys, attorney Relkin said.

Indeed, the FDA notes that all of the reported cases in FAERS of urosepsis and pyelonephritis associated with SGLT2 inhibitors required hospitalizations, and "a few required admission to an intensive care unit or dialysis in order to treat kidney failure."

FDA Also Gives Recommendations to Patients Taking SGLT2 Inhibitors:

"UTIs have been listed in the labels of SGLT2 inhibitors under the section dealing with adverse reactions," attorney Relkin noted. "Moreover, the 'clinical studies experience' section of the label for two of the SGLT2 inhibitors, Invokana (canagliflozin) and Invokamet (canagliflozin and metformin), states that UTIs occurring with the use of these drugs included urosepsis," she added.

However, the FDA is now of the view that listing UTIs as an adverse reaction or under the clinical studies experience sections of SGLT2 inhibitor labels do not provide adequate warning of the potential dangers of SGLT2 inhibitor-associated UTIs.

After reviewing reports pertaining to SGLT2 inhibitors, the FDA determined that warnings needed to be added to the labels to warn about the risks of too much acid in the blood (ketoacidosis) and of serious urinary tract infections potentially leading to life-threatening urosepsis or pyelonephritis, if left untreated.

The FDA recommended patients discontinue use of the SGLT2 inhibitor and immediately seek medical attention if symptoms of ketoacidosis occur, the law firm said. Symptoms of ketoacidosis include nausea, vomiting, abdominal pain, unusual tiredness and trouble breathing.

The FDA also advises patients to contact their health professional "right away" if they develop any signs or symptoms of a UTI, including a burning sensation during urination, feeling the need to urinate frequently, feeling an immediate need to urinate, pain in the pelvic area, blood in the urine, fever, back pain, nausea or vomiting.

In addition to describing these SGLT2-inhibitor safety issues, the FDA's Dec. 4 Safety Communication also provided prescribing and monitoring recommendations.

As well, the FDA indicated that manufacturers of SGLT2 inhibitors would be required to conduct a study to analyze spontaneous postmarketing reports of ketoacidosis in patients using SGLT2 inhibitors, including the collection of additional specialized follow-up data for 5 years.

Weitz & Luxenberg Is Reaching Out to Those Injured While Taking SGLT2 Inhibitors:

SGLT2 inhibitors are FDA-approved prescription medicines for use with diet and exercise to lower blood sugar in adults with type 2 diabetes, according to the FDA.

Besides Invokana (canagliflozin), FDA approval has been granted to these brands of SGLT2 inhibitors:
* Invokamet (canagliflozin and metformin).
* Farxiga (dapagliflozin).
* Xigduo XR (dapagliflozin and metformin extended-release).
* Jardiance (empagliflozin).
* Glyxambi (empagliflozin and linagliptin).
* Synjardy (empagliflozin and metformin).

Weitz & Luxenberg said its investigation of injury cases arising from the taking of SGLT2 inhibitor drugs began last June.

The injury of greatest concern prior to the release of this updated Safety Communication has been SGLT2 inhibitor-caused diabetic ketoacidosis that has resulted in death or has required hospitalization, the firm explained. Now, cases of urosepsis and pyelonephritis that begin as UTIs occurring while taking an SGLT2 inhibitor are equally concerning.

Weitz & Luxenberg said attorneys are available to discuss the legal rights of those taking SGLT2 inhibitors who were injured (or to their surviving spouses or relatives).

To arrange for a no-cost, no-obligation consultation, call Weitz & Luxenberg toll-free at 800-476-6070, or visit the firm's website at http://www.weitzlux.com/ and fill out the request form.

About Weitz & Luxenberg:

Weitz & Luxenberg P.C. is among the nation's leading and most readily recognized personal injury and consumer protection law firms. Weitz & Luxenberg's numerous litigation areas include: mesothelioma, defective medicine and devices, environmental pollutants, products liability, consumer protection, accidents, personal injury, and medical malpractice. Victims of consumer fraud are invited to rely on Weitz & Luxenberg's more than 25 years of experience handling such cases. You can contact the firm's Client Relations department at 800-476-6070 or at info@weitzlux.com.

More information: http://www.weitzlux.com/.

Twitter: @WeitzLuxenberg

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/weitz-luxenberg-adds-serious-urinary-tract-infections-to-sglt2-inhibitor-injuries-probe-2015-1207-05.shtml.

NEWS SOURCE Weitz and Luxenberg P.C. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.

Harbor Compounding Pharmacy Advises About Coverage for Compounded Medications During Open Enrollment 2016

compounded medications

COSTA MESA, Calif., Oct. 12, 2015 (SEND2PRESS NEWSWIRE) -- Many insurance plans are dropping coverage of compounded medications, but some insurance plans still do cover for these custom formulations. Harbor Compounding Pharmacy provides resources and referrals to patients to find insurance coverage for their compounded medications during open enrollment 2016.

Healthcare open enrollment is coming up from November 1, 2015 to January 31, 2016, and many patients on compounded medications are wondering if their current insurance, or any insurances at all, will cover for compounded medications. In the past, most insurance plans included coverage of compounded medications. However in the past few years, insurance coverage for compounded medications has been dwindling, but there is hope. There are some existing insurance plans that still cover for some compounded medications.

Harbor Compounding Pharmacy has helped many patients try to understand insurance coverage for their compounded medications. If patients are wondering if their plan covers for compounded medications, they must inquire if the plan covers for compounded medications made from "bulk ingredients." This means the insurance plan will cover for compounded medications that are made from pure ingredients, in other words made from scratch. Harbor Compounding Pharmacy also suggests patients call their insurance agents and further inquire if they have had experience signing up patients with compounded medications and have those compounded medications successfully covered by any insurance plan.

Harbor Compounding Pharmacy is currently working with select California insurance agents with experience finding coverage for compounded medications for their patients. If patients are on compounded medications and are in need of a referral to an insurance agent, the patient can contact the pharmacy or go to the pharmacy website to find out who is available to service them. Because insurance plans vary from state to state across the country, patients must work with insurance agents who are familiar with the insurance plans within their state. Harbor Compounding Pharmacy is continuing to look for partnerships with insurance agents experienced in finding coverage for compounded medications.

Overall, insurance coverage for compounded medications may be limited, but it is not impossible to find a plan that will cover for these custom compounded formulations. Open enrollment may seem far off, not ending until January 31, 2016, but doing the research to find the right insurance plan can be a lengthy process, thus patients should start inquiring as soon as possible. Harbor Compounding Pharmacy is open to helping current and new patients connect to the right resources and to the right people to make this process easier. If patients have questions regarding if their existing insurance plan covers for compounded medications at all, they should contact the pharmacy.

More information: http://harborcompounding.com/.

Twitter: @harborrx

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/harbor-compounding-pharmacy-advises-about-coverage-for-compounded-medications-during-open-enrollment-2016-2015-1012-07.shtml.

NEWS SOURCE Harbor Compounding Pharmacy :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.

E-VAI – the Artificial Intelligence Platform from Eularis Changes the Rules of the Marketing in Pharma

E-VAI platform

NEW YORK, N.Y. and Tokyo, Sept. 15, 2015 (SEND2PRESS NEWSWIRE) -- Eularis announces today the release of E-VAI, the latest development in sophisticated artificial intelligence technology delivering next generation analytics and decision making to Pharma marketers globally. E-VAI changes the game for marketers struggling to understand and get value from their marketing.

For a number of years now, all eyes have been pointing towards the powers of Artificial Intelligence (AI) in business. Eularis to brings this advanced technology into Pharma marketing to reverse the trend of poor marketing and sales results and decreasing budgets. E-VAI takes the same data but delivers more accurate results, faster and provides answers to the questions that marketers need.

Dr. Andree Bates, founder and CEO of Eularis says, "Marketing executives must continuously make complex decisions and the increase in channels, and the market environment itself makes it very difficult to get this right without the intervention of something as sophisticated as AI."

Eularis has used the brains of top Professors in the field. A comparison of the AI results with those delivered by linear approaches shows much higher accuracy and far superior understanding of synergistic effects.

Prof. Lang, Mathematician, Theoretical Physicist and Data Scientist, when studying the results had this to say: "What Eularis has developed for the Pharma Industry is a thing of beauty. The underlying algorithms are so cutting edge they did not exist 3 years ago. I can safely say that Eularis is the first company in the world to offer this level of sophisticated machine learning based tools, using a live customer focused environment to ensure stronger financial results."

E-VAI is available now globally and has already been tested on a number of projects across multiple portfolios and markets.

About Eularis:

Eularis is the leading provider of next generation advanced marketing analytics to the Pharmaceutical market. The artificial intelligence powering Eularis analytics enables marketing, analytics and sales executives to achieve faster brand success. Since 2003 the company has developed significant experience in the global pharmaceutical market through client engagements with Boehringer-Ingelheim, Merck, Pfizer, Roche, and many others. To learn about Eularis go to http://www.eularis.com/.

Twitter: @EULARIS

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/e-vai-the-artificial-intelligence-platform-from-eularis-changes-the-rules-of-the-marketing-in-pharma-2015-0915-01.shtml.

NEWS SOURCE Eularis :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.

Zofran Birth Defect Cases Being Accepted by Weitz and Luxenberg

consumer protection law

NEW YORK, N.Y., April 7, 2015 (SEND2PRESS NEWSWIRE) -- Weitz & Luxenberg, P.C., announced it is accepting cases of congenital heart defects and cleft facial abnormalities in children whose mothers took the prescription drug Zofran during pregnancy to relieve symptoms of morning sickness.

Zofran - generic name ondansetron - has never been approved by the U.S. Food & Drug Administration (FDA) for treatment of morning sickness symptoms and medical studies have linked Zofran use during the first trimester of pregnancy to birth defects, the law firm said.

Weitz & Luxenberg added that approximately 1 million women take Zofran or ondansetron each year to relieve the symptoms of morning sickness, specifically nausea and vomiting.

Zofran is FDA-approved for use by cancer patients to prevent the nausea and/or vomiting that can accompany chemotherapy and that can occur after an operation, the firm explained.

However, Zofran has not been approved by the FDA to prevent or treat morning sickness in pregnant women.

Zofran Maker Accused by U.S. Justice Dept.:

In 2012, the manufacturer of Zofran - pharmaceutical giant GlaxoSmithKline - paid a fine of $1 billion as part of a settlement of claims brought by the U.S. Department of Justice, Weitz & Luxenberg said.

The Justice Department claimed, among other things, that GlaxoSmithKline illegally promoted certain forms of Zofran for the treatment of morning sickness in pregnant women, and paid doctors to promote and prescribe Zofran, the firm indicated.

Despite that settlement, GlaxoSmithKline still faces civil liability. Weitz & Luxenberg said it is moving forward with efforts to hold GlaxoSmithKline accountable by accepting cases where women who took Zofran in the first trimester of pregnancy gave birth to children with congenital heart defects and/or cleft lip, cleft palate or both.

Free Consultation For Zofran Birth Defect Victims:

The law firm said Zofran victims can contact Weitz & Luxenberg for a no-cost, no-obligation discussion of their legal rights to compensation from Zofran's maker.

The free consultation can be arranged by contacting Weitz & Luxenberg toll-free at 844-400-HELP or online at www.weitzlux.com, the firm said.

In addition to wanting to hear from mothers who took Zofran, Weitz & Luxenberg also expressed interest in exploring the legal rights of men and women born with a potentially Zofran-related birth defect who this year are between the ages of 18 and 24.

About Weitz & Luxenberg:

Weitz & Luxenberg P.C. is among the nation's leading and most readily recognized personal injury and consumer protection law firms. Weitz & Luxenberg's numerous litigation areas include: mesothelioma, defective medicine and devices, environmental pollutants, products liability, consumer protection, accidents, personal injury, and medical malpractice. Victims of consumer fraud are invited to rely on Weitz & Luxenberg's more than 25 years of experience handling such cases. You can contact the firm's Client Relations department at 800-476-6070 or at clientrelations@weitzlux.com.

More information: http://www.weitzlux.com/.

Twitter: @WeitzLuxenberg

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/zofran-birth-defect-cases-being-accepted-by-weitz-and-luxenberg-2015-0407-07.shtml.

NEWS SOURCE Weitz and Luxenberg P.C. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.

Weitz & Luxenberg’s Relkin Appointed to Xarelto MDL Leadership Team

mass-tort litigations

NEW YORK, N.Y., Feb. 11, 2015 (SEND2PRESS NEWSWIRE) -- Ellen Relkin, of counsel attorney with Weitz & Luxenberg, P.C., has been named to the plaintiffs' steering committee created by judicial order to facilitate lawsuits against the makers of the anticoagulant drug Xarelto, the personal injury and mass tort law firm today announced.

The Hon. Eldon E. Fallon of the U.S. District Court for the Eastern District of Louisiana selected Ms. Relkin along with 11 other attorneys to serve on the committee. They are tasked with helping ensure that the many Xarelto lawsuits heard by Judge Fallon proceed with optimum efficiency, Weitz & Luxenberg said.

Those lawsuits were already on track to receive efficient handling - late last year they were consolidated into a multidistrict litigation, the firm noted.

The litigation since then has been officially known as In Re: Xarelto (Rivaroxaban) Products, MDL No. 2592. Ms. Relkin will serve on the plaintiffs' steering committee for at least a one-year term, according to the judicial order.

Ms. Relkin was chosen to serve on the committee in part because of her past proven strong leadership skills; in other mass-tort litigations she has served or continues to serve on plaintiffs' steering committees or in the role of liaison counsel, Weitz & Luxenberg indicated.

Xarelto Side Effects:

Xarelto became the subject of a large number of lawsuits because some patients who take it suffer potentially dangerous side effects, such as the risk of unstoppable bleeding, the firm said.

Anticoagulant Xarelto may be prescribed to reduce the risk of deep-vein thrombosis and pulmonary embolism, especially following knee or hip replacement surgery. Xarelto may also be prescribed to prevent strokes and other clotting events related to atrial fibrillation, Weitz & Luxenberg explained.

Ms. Relkin has been at the forefront of the firm's actions against the makers of Xarelto, which positions her to understand the many intricacies of these cases, the firm said.

As a member of the MDL plaintiffs' steering committee, Ms. Relkin will help conduct all pretrial discovery, coordinate trial team selection, explore all settlement options, and keep the plaintiffs' attorneys who are not on the steering committee apprised of developments in the MDL, the judicial order specified.

Experienced Litigator:

Ms. Relkin began the practice of law in 1984, following completion of legal studies at Rutgers University Law School. She is admitted to practice law in four jurisdictions: New Jersey, New York, Pennsylvania and the District of Columbia. In New Jersey, Ms. Relkin holds state Supreme Court-issued certification as a Civil Trial Attorney, the firm reported.

Weitz & Luxenberg said the focus of Ms. Relkin's practice is pharmaceutical/medical-device product liability and environmental toxic torts. Ms. Relkin has amassed many honors over the years, including designation as both a New Jersey and New York "Super Lawyer."

Ms. Relkin, the firm said, is a member of many prestigious organizations for attorneys and serves in leadership positions within several of them. Most notably, she holds a post on the Board of Governors of the New Jersey Association for Justice.

Ms. Relkin also is a coveted speaker at professional gatherings of attorneys. She has authored and co-authored a number of law journal articles and treatise chapters, Weitz & Luxenberg said.

About Weitz & Luxenberg:

Weitz & Luxenberg, P.C., is among the nation's leading and most readily recognized personal injury law firms. Weitz & Luxenberg's numerous litigation areas include: mesothelioma, defective medicine and devices, environmental pollutants, consumer protection, accidents, personal injury, and medical malpractice. Victims of accidents are invited to rely on Weitz & Luxenberg's more than 25 years of experience handling such cases. You can contact the firm's Client Relations department at 800-476-6070 or at clientrelations@weitzlux.com.

More information: http://www.weitzluxenberg.com/.

To view the original version on Send2Press Newswire, visit: https://www.send2press.com/newswire/weitz-luxenberg-relkin-appointed-to-xarelto-mdl-leadership-team-2015-0211-002.shtml.

NEWS SOURCE Weitz and Luxenberg, P.C. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by and Copr. © 2015 Send2Press® Newswire, a service of Neotrope®.