Ad
related to: health, fda- Contact Us
Call + Email
24/7 Live Chat
- Verify: FDA Registration
Free Tool To Verify That Your US
FDA Registration Is Currently Valid
- Food & Beverage
Full Service
Everything You Need
- FDA Registration
Quick & Easy
Register Your Business
- Contact Us
Search results
Psychedelic drug MDMA faces questions as FDA considers approval for PTSD
WMBF News Myrtle Beach· 2 hours agoFederal health regulators are questioning the safety and evidence behind the first bid to use MDMA,...
FDA approves Moderna’s mRNA RSV vaccine for older adults
CNN via Yahoo News· 2 hours agoThe US Food and Drug Administration has approved another vaccine that can help protect older people...
JD Supra: FDA Makes Good on Its Promise to Regulate Laboratory-Developed Tests
JD Supra· 49 minutes agoYesterday, the Food & Drug Administration (“FDA” or “the Agency”) issued a highly anticipated – and highly controversial – final rule, which rolls out a four-year, five-stage ...
FDA Extends Review Deadline For Regeneron/Sanofi's Dupixent For 'Smoker's Lungs' Disease
Benzinga via Yahoo Finance· 5 hours agoOn Friday, the FDA extended the target action date of priority review of supplemental application...
FDA responds to senator’s letter that calls out ‘FDA’s failure to act’ on NOW’s test results
Nutraingredients.com· 5 hours agoRobert Califf, asking for clarification on several dietary supplements issues, with much of the...
FDA reveals food oversight restructure in wake of infant-formula crisis
Just Food via Yahoo Finance· 9 hours ago“This reorganisation has been a major undertaking for the FDA, and I am proud of what we will be...
US FDA staff raises concerns over data from MDMA-based PTSD therapy
Reuters via AOL· 8 hours ago(Reuters) -The U.S. health regulator's staff said on Friday data on the psychedelic drug MDMA for...
FDA sets review date for Iterum's urinary infection drug By Investing.com
Investing.com· 3 hours agoIterum Therapeutics plc (NASDAQ:ITRM), a clinical-stage pharmaceutical company, announced today that...
FDA Updates Fiji Recall, Downgraded To Class 3
Black Enterprise· 7 hours agoDuring the week of May 20, the FDA adjusted its concern to a Class III, which dictated that there is no relative risk of adverse health consequences. As...
Guest column: With FDA approval of software treatment for depression, the digital medicine...
WRAL TechWire· 10 hours agoIn a watershed moment for digital health innovation, the FDA recently granted clearance to Rejoyn, a...
