PHARMACY

MediSafe updates medication reminder app to allow automatic refills

BY Alaric DeArment

HAIFA, Israel — Users of a medication-management app can now refill their prescriptions using an enhancement to it.

MediSafe announced Monday an updated version of its Medication Refill Reminder app allowing users to enter contact information for their preferred pharmacies and, once alerted that a medication refill is needed, to click on the pharmacy logo that directs them to the mobile refill page of the specified pharmacy. The app currently supports refills for Walgreens, CVS, Rite Aid and Health Mart.

"One key issue tied to non-adherence is people’s forgetfulness when it comes to refilling medications, which is why we implemented this new option to make it easier for users to act instantly when a reminder is sent," MediSafe CEO Omri Shor said. "Our mobile solution plays an important supportive role in helping people manage their medications properly, as well as their families, which motivates us to continuously update and make our applications more personalized and convenient for every user."

 

keyboard_arrow_downCOMMENTS

Leave a Reply

No comments found

TRENDING STORIES

PHARMACY

Regeneron Pharmaceuticals, Geisinger Health System form partnership in major genetics initiative

BY Alaric DeArment

TARRYTOWN, N.Y. — A drug maker has started a program to find the genetic determinants of human disease and speed the discovery and development of new drugs. The program includes a five-year project that it said would be one of the largest of its kind in terms of the number of patients involved.

Regeneron Pharmaceuticals and Geisinger Health System, which serves about 3 million patients, have recruited more than 100,000 patient volunteers for the project, in which Geisinger will collect samples from them and Regeneron will perform sequencing and genotyping to generate genomic data. The goal of the project is to improve patient care and help drug discovery and development.

"Genetics has been at the core of our research efforts at Regeneron since its early days," Regeneron president and chief scientific officer George Yancopoulos said. "In fact, our first [Food and Drug Administration-approved] therapy treats a rare genetic disorder, and the target of one of our product candidates in late-stage development that acts to lower LDL cholesterol was identified using human genetics. With the tremendous recent advances in DNA sequencing, we believe that now is the time to increase our commitment to and invest in human genetics research."

Regeneron will use its research and functional biology capabilities to find associations between genes and disease, while Geisinger will collect samples using its MyCode repository and electronic medical records.

The collaboration between the two companies is part of a larger human genetics initiative through Regeneron’s subsidiary, the Regeneron Genetics Center, which also has partnerships in place with the National Institutes of Health’s National Human Genome Research Institute, and plans are in place to develop relationships with other academic, government and medical systems.

"Regeneron has always believed in the power of genetics to help shape our understanding of disease and to guide development of novel therapeutics," Yancopoulos said. "However, there have been major limitations that have prevented optimal utilization of human genetics at a large scale. We believe that we can now address these limitations and that now is the time to increase our investment in human genetics."

 

keyboard_arrow_downCOMMENTS

Leave a Reply

No comments found

TRENDING STORIES

PHARMACY

FDA cites Ranbaxy plant for possible violations

BY Alaric DeArment

GURGAON, India — The Food and Drug Administration has found possible violations of agency regulations at a manufacturing plant in India owned by drug maker Ranbaxy Labs, the company said Monday.

Ranbaxy said it received a Form 483 from the FDA, a statement issued to a company’s management after it has inspected a plant and found conditions that may violate the agency’s regulations, and that products produced therein could be hazardous to people who use them. The plant in question is in Toansa, in India’s Punjab region.

"Ranbaxy continues to improve its systems and processes and remains fully committed to upholding the highest standards that patients, prescribers, regulators and all other stakeholders expect from the Company," a statement from the drug maker read. "Ranbaxy stays firmly committed to its philosophy of ‘Quality and Patients First.’"

In September, the FDA barred importation of drugs from the company’s plant in Mohali, also in Punjab, through an import alert, meaning customs officials can seize drugs from the plant when they reach the U.S. border. The agency said the alert would remain in effect until Ranbaxy complied with the FDA’s current good manufacturing practices, or CGMP. Two other Ranbaxy plans in India, Paonta Sahib and Dewas, have been under import alerts since 2008.

 

keyboard_arrow_downCOMMENTS

Leave a Reply

No comments found

TRENDING STORIES