The FDA Is Launching New Traceability Rules for Added Food Safety — and Everyone Is Confused
On January 20, 2026, the Food and Drug Administration's (FDA) new traceability rules — dubbed the Food Traceability Final ...
GMA Network3 天
FDA creates task force to enhance medical devices regulation
The Food and Drug Administration (FDA) has formed a task force assigned to improve regulation of medical devices in the ...
Medscape11 天
FDA Faces Blowback Over Stricter Regulation of Lab-Developed Tests
Clinical laboratory lobbying groups are suing the FDA over its plans to more strictly regulate lab-developed tests. For now, ...
Severity of various FDA product recalls including Class I which can cause death, serious ...
Hundreds of foods are recalled by the FDA every year. Food recalls could fall into different categories, depending on how ...
A New Era For Kratom: What The Latest FDA Study Reveals About Kratom Leaf
For years, kratom has been clouded by controversy, largely fueled by media portrayals that paint a negative picture of this ...
Food Safety News38 分钟
FDA issues warning letters to seafood and produce distributors for import violations
The Food and Drug Administration sends warning letters to entities under its jurisdiction as part of its enforcement activities. Some letters are not ...
Column: A federal appeals court hands the FDA a stupendous win in its battle against stem ...
The FDA claimed these clinics were plying patients with an illegal drug derived from their stem cells. A federal court agrees ...
medtechintelligence17 天
New FDA Regulations for Laboratory Developed Tests (LDTs): What it Means to Laboratories
As laboratories navigate the evolving landscape of Laboratory Developed Tests (LDTs), the FDA’s phased approach to regulation ...
US FDA approves IntraBio's drug for rare genetic disease
The U.S. Food and Drug Administration approved IntraBio's drug for a rare and fatal genetic disorder, the health regulator ...
philstar.com4 天
FDA task force to enhance regulation of medical devices
The country's Food and Drug Administration has established Task Force Obsidian, a technical working group aimed at enhancing the regulation of medical devices.
NBC New York24 天
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays, AP finds
The FDA didn’t open its first overseas outposts until 2008, after dozens of U.S. deaths were linked to a contaminated blood ...