The move marks an advancement in reducing plastic waste and assisting global brands in achieving their sustainability ...
To be a person in the year 2025 is to encounter, in one way or another, the marketing onslaught for compounded ...
Doron Therapeutics, a clinical-stage biotechnology company based in Chapel Hill, has received a Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration ...
President Donald Trump's nominee to lead the Food and Drug Administration (FDA), Dr. Marty Makary, passed a key committee vote on Thursday morning.
Activists have slammed the GRAS program, arguing it allows companies to "self-certify" the safety of food additives.
The agency’s approach to GRAS determinations has evolved over the intervening decades, with the last major change coming in 2016 with the publication of what is referred to as the final GRAS rule.
Dyne Therapeutics’ DYNE-101 shows positive results in phase 1/2 ACHIEVE study. Read why DYN stock may rise with FDA approval and a $2.78B market opportunity.
FLORHAM PARK, N.J., March 13, 2025 (GLOBE NEWSWIRE) -- Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage clinical ...
U.S. Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. directed the U.S. Food and Drug Administration (FDA) to explore potential rulemaking opportunities to tighten or ...
John Arena is interim president of global pharma services at Cencora, managing a team that offers a broad range of solutions ...
Providers across Missouri are resuming abortion services, months after voters approved a measure to enshrine reproductive rights in the state constitution.