FDA warns of scramble for work and parking space in Monday return to office
The U.S. Food and Drug Administration told staff this week it cannot guarantee work space or parking spots among the hurdles ...
RFK Jr. wants to eliminate FDA’s controversial food additive program. Here’s why that matters
It’s time to revamp the FDA’s “generally recognized as safe,” or GRAS, program that allows companies to add untested ...
FDA Recalls Acne Products For Possible Contamination and Risk of Cancer-Causing Chemicals
The US Food and Drug Administration has recalled six skincare products from popular brands due to benzene contamination, which is linked to cancer risk. The FDA emphasised that the cancer risk to ...
FDA warns of scramble for workspaces and parking spots in Monday return to office
The U.S. Food and Drug Administration told staff this week it cannot guarantee workspaces or parking spots when they return ...
HHS Secretary RFK Jr. orders FDA to close food ingredients loophole
Health and Human Services Secretary Robert F. Kennedy Jr. ordered the Food and Drug Administration on Monday to revise its ...
Kennedy Rattles Food Companies With Vow to Rid Food of Artificial Dyes
Mr. Kennedy told executives of major food companies that he wants synthetic colors removed from their products. “Decision ...
C&EN1d
Kennedy orders FDA to review food ingredient loophole
US Health and Human Services secretary Robert F. Kennedy Jr. directs the Food and Drug Administration to explore revamping ...
The Cool Down on MSN2h
RFK Jr. drops threat on major food corporations — and shoppers may soon see the impact
"We look forward to continued engagement ... to support public health, build consumer trust and promote consumer choice." RFK ...
Some La Roche-Posay, Proactiv and Walgreens acne treatments recalled due to benzene levels
The Food and Drug Administration is asking retailers to remove a small number of acne creams from their shelves that contain ...
The BMJ1d
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study
Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...