Abbott (NYSE:ABT) is facing an FDA warning letter alleging quality system regulation violations related to FreeStyle Libre CGM production.
In an era of increasing product complexity, FDA scrutiny, and compressed development cycles, medical device teams rely on milestones to guide progress. Yet too often, those milestones are managed in ...
Industry embraced prevention, but inspections, enforcement and information-sharing have struggled to keep pace. Fifteen years in, experts debate what FSMA has delivered — and what it hasn’t.
FDA’s new PreCheck pilot streamlines building US pharma manufacturing plants with earlier guidance and faster reviews. Read more here.
The FDA launched PreCheck pilot program to strengthen U.S. drug supply chain by improving regulatory predictability.
The program will allow for frequent communication with the FDA, giving manufacturers timely input and guidance regarding the ...
Two Teton County, Idaho, men were arrested after law enforcement executed simultaneous search warrants at two Victor-area ...
The guidelines will help clinicians determine whether patients seeking care via telehealth and virtual visits need urine tests or empiric antibiotics.
LOS ANGELES, CA - January 15, 2026 - PRESSADVANTAGE - Muse Treatment Alcohol & Drug Rehab Los Angeles has released ...
CHARLESTON, W.Va. — West Virginia officials on Tuesday introduced the state’s 2026 vacation guide, highlighting new travel ...
The US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) just issued a joint statement outlining 10 “Guiding Principles” ...
WASHINGTON, D.C. — The U.S. Food and Drug Administration is moving on two fronts to strengthen consumer protection, launching ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results