Ads
related to: fda- Contact Us
Call + Email
24/7 Live Chat
- Food & Beverage
Full Service
Everything You Need
- Verify: FDA Registration
Free Tool To Verify That Your US
FDA Registration Is Currently Valid
- FDA Registration
Quick & Easy
Register Your Business
- Contact Us
Search results
Eli Lilly Alzheimer’s drug gets FDA panel date after approval delay
The Hill via AOL· 2 hours agoAn outside panel of advisers to the Food and Drug Administration (FDA) will meet next month to...
FDA under fire: Pared-down LDT Final Rule leaves unanswered questions | JD Supra
JD Supra· 11 hours agoFDA has finalized its landmark proposed rule that will amend the definition of “in vitro diagnostic (IVD) products” in 21 CFR § 809.3 to make explicit that IVDs are medical ...
FDA sets date for advisory meeting on Lilly’s closely watched Alzheimer’s drug
BioPharma Dive via Yahoo Finance· 6 hours agoThe advisory committee meeting is scheduled for June 10. During it, experts in the fields of...
US FDA panel to discuss Eli Lilly Alzheimer's drug on June 10
Reuters via Yahoo News· 4 hours agoFood and Drug Administration's approval last year. Lilly's donanemab was declined accelerated...
FDA Experts Weigh In On Incannex's CannQuit-O With Feedback On CBD As Treatment For Opioid Use...
Benzinga· 1 hour agoHealthcare Inc. IXHL, a cannabinoid and psychedelic medicine biotechnology company, announced the...
The End of an Era? FDA Finalizes LDT Rule But Grandfathers Many Existing LDTs | JD Supra
JD Supra· 11 hours agoOn May 6, 2024, the Food and Drug Administration (FDA) published its final rule for laboratory developed tests (LDTs). The final rule cemented the agency’s forecasted decision ...
FDA advisers to weigh first psychedelic therapy in early June
FierceBiotech· 3 hours agoLykos Therapeutics’ MDMA-assisted therapy is charting yet another first in the psychedelic field: an...
FDA set to discuss order renewal for Swedish Match products
Winston-Salem Journal· 30 minutes agoThe Food and Drug Administration said Tuesday that its Tobacco Products Scientific Advisory Committee will meet on June 26 to discuss the renewal of a risk modification order submitted by
FDA panel to consider MDMA for PTSD treatment
NBC NEWS· 2 hours agoThis would be the first FDA panel of outside experts to review a potential new PTSD treatment in 25 years. PTSD is a disorder caused by very stressful...
Inflation’s hit to the FDA
Politico· 2 hours agoCHECK-IN WITH CAVAZZONI — The FDA’s top drug regulator wants Congress to know that flat taxpayer funding is forcing the FDA to make choices about how it ...
Ad
related to: fda