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US FDA advisers to consider if new COVID shots should target JN.1 variant
AOL· 10 hours agoThe FDA reviewers said since the difference between JN.1 and newer subvariants such as KP.2 subvariants is not much, it is possible that vaccines developed against JN.1 may adequately protect against KP.2.
BrainsWay Receives Expanded FDA Labeling to Treat Late Life Depression - BrainsWay (NASDAQ:BWAY)
Benzinga· 11 hours ago...NASDAQ & TASE: BWAY) ("BrainsWay" or the "Company"), a global leader in advanced noninvasive neurostimulation treatments for mental health disorders, today announced that the US Food and Drug Administration (FDA) has granted an expanded indication for the Company's Deep Transcranial Magnetic...
Cucumbers Recalled in 14 States for Possible Salmonella
allrecipes via Yahoo News· 8 hours agoCheck your supply! Getty/Allrecipes The U.S. Food & Drug Administration (FDA) announced that...
FDA urged to relax decades-old tissue donation restrictions for gay and bisexual men
Denver Post· 1 day agoThe federal government in 2020 and 2023 changed who it said could safely donate organs and blood,...
FDA Conditionally Approves Eli Lilly's Thyroid Cancer Drug For Pediatric Patients With Certain...
Benzinga via AOL· 5 days agoWednesday, the FDA granted accelerated approval to Eli Lilly And Co’s (NYSE:LLY) selpercatinib...
Psychedelic drug MDMA faces questions as FDA considers approval for PTSD
ABC7 New York· 1 day agoThe Food and Drug Administration posted its initial review of the drug Friday, ahead of a meeting of...
FDA approves Moderna's RSV shot for older adults
Becker’s Hospital Review· 16 hours agoThe FDA has given the green light to Moderna's mRNA-based respiratory syncytial virus vaccine, specifically for older adults, the drugmaker announced May 31. "This approval ...
Ground black pepper recalled nationwide over possible salmonella contamination
KSNT Topeka· 43 minutes agoA pepper product is being recalled nationwide over salmonella.
Lawsuit Filed Challenging FDA Final Rule Regulating Laboratory Developed Tests | JD Supra
JD Supra· 16 hours agoAs detailed in our prior analysis (here), the final rule amended the FDA’s existing regulations to make explicit the agency’s interpretation that LDTs are “devices” under ...
FDA Considers a Big Change to Decaf Coffee
newser· 1 day agoThe request: Groups including the Environmental Defense Fund petitioned the FDA to ban the carcinogen, which is used "in many different industries...