General Discussion
Related: Editorials & Other Articles, Issue Forums, Alliance Forums, Region ForumsNYT: Eli Lilly Chief Says He Will Fight for the F.D.A., Challenging Kennedy's Stance
The health care giants David Ricks defended the agencys role in reviewing data and ensuring drug safety.
By Aimee Ortiz
Dec. 4, 2024, 4:21 p.m. ET
President-elect Donald J. Trumps pick of Robert F. Kennedy Jr., a longtime vaccine skeptic with no medical or public health training, to be the next health secretary has sent a chill through the American public health sphere.
Among drugmakers, there are already signs of pushback.
David Ricks, the chair and chief executive of Eli Lilly, speaking at The New York Timess DealBook Summit, said his $750 billion company would fight to defend preserving the Food and Drug Administration as it stands today.
Were the only country on Earth that does primary data review, Mr. Ricks said, explaining that when the company creates data, only the F.D.A. reviews every digit of that data.
I think thats a value to society we need to keep, he said. Well argue that strongly with our new regulator.
Mr. Kennedy posted his plans for the F.D.A. on social media in late October, days before President-elect Trumps Election Day win and his subsequent nomination of Mr. Kennedy to lead the Department of Health and Human Services.
/snip
Mike 03
(17,135 posts)My rec doesn't mean I love Eli Lilly or 100% trust its CEO.
rich7862
(229 posts)Dennis Donovan
(26,796 posts)...and he's Big Pharma!
BeyondGeography
(40,051 posts)Almost didnt recognize it.
WarGamer
(15,621 posts)bucolic_frolic
(47,316 posts)probably 60-70 years on this evolving method.
FDA and Clinical Drug Trials: A Short History
https://www.fda.gov/media/110437/download
The 60 day approval "default" under the 1938 Act was removed. New drugs had to have positive and specific, and increasingly detailed approval from FDA to go to market and FDA was given the authority to set standards for every stage of drug testing from laboratory to clinic.
Milestones in U.S. Food and Drug Law
https://www.fda.gov/about-fda/fda-history/milestones-us-food-and-drug-law
1800-1899: FDA Milestones
1820 Eleven physicians meet in Washington, D.C., to establish the U.S. Pharmacopeia, the first compendium of standard drugs for the United States.
1848 Drug Importation Act passed by Congress requires U.S. Customs Service inspection to stop entry of adulterated drugs from overseas.
1862
Charles M Wetherill
President Lincoln appoints a chemist, Charles M. Wetherill, to serve in the new Department of Agriculture. This was the beginning of the Bureau of Chemistry, the predecessor of the Food and Drug Administration.
1880 Peter Collier, chief chemist, U.S. Department of Agriculture, recommends passage of a national food and drug law, following his own food adulteration investigations. The bill was defeated, but during the next 25 years more than 100 food and drug bills were introduced in Congress.
erronis
(16,989 posts)then it makes their lives harder.
Might as well be in a third-rate country..... Oh, wait.
groundloop
(12,337 posts)For the time being we can take all the help we can get to dampen the orange clown's effects on American society.
Karasu
(286 posts)Both are equally unqualified (a prerequisite for this administration), and both are sex predators. Hell, Kennedy should have at LEAST as much, considering how absurd his views on science and health are...but of course, the GOP is fucking trash.
It is completely insane to me that for some reason he's been given a fucking pass and everyone is just treating his appointment as an inevitability.
TBF
(34,565 posts)The pharma industry is not letting go easily.
Seeking Serenity
(3,045 posts)After years and years of cussing them. Big Pharma, like Big Food, Big Oil, Big Banking, etc, etc, is not your friend.
Sorry not sorry.