FDA commissioner Marty Makary said it would be “magical” for consumers to see prescription drugs on pharmacy shelves instead ...

A new study published in Therapeutic Innovation & Regulatory Science provides crucial insights into the design and ...

Cedars Sinai build drug safety AI tool to forecast drug toxicity using patient avatars and EHR data, aiming to reduce ...

Questions remain among top Food and Drug Administration officials over who has the appropriate legal authority to sign off on ...

A new study co-written by a University of Illinois Urbana-Champaign expert in operations management finds that drugs approved ...

The U.S. Food and Drug Administration has delayed reviews of two drugs chosen for the Trump administration's new fast-track ...

US Food and Drug Administration layoffs appear to be affecting programs that track drug safety. Fired workers from the Division of Drug Information, which conducts safety monitoring, say the DDI team ...

Generic drugs account for more than 90 percent of prescriptions filled in the United States. Recent studies have found concering variability in quality and safety America’s generic drug supply, most ...

The FDAAA did not significantly alter the overall time to first postmarket safety action for novel therapeutics. Earlier safety actions were observed within the first five years post-approval, ...

January 10, 2026 - PRESSADVANTAGE - WhiteSands Alcohol & Drug Rehab Ocala has published a new medically focused ...

The U.S. Food and Drug Administration has released a proposal on how it plans to handle safety issues related to marketed drugs. Significant safety issues related to post-market drugs include serious ...

Inductive Bio, an AI drug discovery partner developing virtual chemistry labs, received an up to $21M award to lead a project to develop next-generation models of drug toxicity to advance safer ...