‘Miracle’ supplement recalled nationwide over death, diarrhea risks
A supplement described as from a “miracle tree” by a nutritional therapist has been recalled because of possible…
Disc Medicine Receives Complete Response Letter from FDA for Bitopertin for the Treatment of EPP
Disc Medicine Inc FDA acknowledged that AURORA and BEACON provided sufficient evidence that bitopertin significantly lowers PPIX and…
Hims & Hers compounder received FDA warning letter| STAT
The Food and Drug Administration late last year issued a warning letter to MedisourceRx, a compounding pharmacy owned…
Germany Bans Amazon from Price Controls
This Week’s Regulatory Updates Germany bans Amazon price caps: The Bundeskartellamt demands Amazon halt anti-competitive pricing and repay…
Marty Makary addresses staff concerns over drug voucher program
WASHINGTON — At an employee town hall on Tuesday, Food and Drug Administration leaders tried to quell staff…
Will 2026 FDA Decisions on Afrezza and FUROSCIX Redefine MannKind’s (MNKD) Narrative
Earlier in January, MannKind Corporation outlined upcoming 2026 regulatory milestones, including FDA decisions on Afrezza label updates, a…
FDA Goon Delivers Wild Take on Prescription Drug Safety
FDA commissioner Marty Makary said it would be “magical” for consumers to see prescription drugs on pharmacy shelves…
NRx submits 70,000-patient ketamine data to US FDA
NRx Pharmaceuticals (Nasdaq: NRXP) will submit real-world evidence from over 70,000 patients treated with intravenous ketamine…
Tylenol, Advil, Purina, Haribo face urgent FDA recall
While a car recall is one notice I never ignore, I can’t ever remember throwing out a single…
FDA Accepts for Review INOVIO’s BLA for INO-3107 for the Treatment of Adults with Recurrent Respiratory Papillomatosis (RRP)
PLYMOUTH MEETING, Pa., Dec. 29, 2025 /PRNewswire/ — INOVIO (NASDAQ: INO), a biotechnology company focused on developing and…