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 ...
These Food Additives in Your US Food Are Banned in Europe—See the List
Many Americans have started to question the quality of ingredients used within their food, some of which are banned in Europe ...
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 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 ...
Trump administration withdraws nomination of David Weldon for CDC director
A person familiar with the matter said the White House pulled the nomination because it became clear Weldon did not have the ...
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 ...
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 ...
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 ...
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 ...