The Food Safety and Standards Authority of India has opened registrations for the 11th Food Analyst Examination 2025–26, with ...
Announces Plans to Cancel Equity Line Upon S-3 EffectivenessMove to Shelf Registration Statement Enables More Cost-Effective Capital ...
The U.S. Food and Drug Administration has approved Exdensur (depemokimab-ulaa) as an add-on maintenance treatment for severe ...
INB-619, IN8bio’s novel gamma-delta ('γδ”) T cell engager through an Investigational New Drug ('IND”) application ...
For decades, the FDA made it nearly impossible to know which factories were manufacturing your generic medications. ProPublica built a tool to show you. Here’s how we did it.
Ameluz® and RhodoLED® New Drug Application (NDA) and Investigational New Drug Application (IND) have successfully been transferred to ...
Moleculin Biotech, Inc., (Nasdaq: MBRX) ('Moleculin” or the 'Company”), a late-stage pharmaceutical company with a broad ...
TEMPO.CO, Jakarta - The Food and Drug Monitoring Agency (BPOM) has issued the first generic drug permit in Indonesia containing dydrogesterone for infertility treatment. With the presence of generic ...
U.S. health regulators sent warning letters Wednesday to 18 websites selling counterfeit or unapproved versions of Botox and similar injectable drugs commonly used to smooth wrinkles. The Food and ...
WASHINGTON — Federal officials have approved another generic version of the abortion pill mifepristone, a regulatory formality that quickly triggered pushback from anti-abortion groups and politicians ...