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 ...
The FDA is expected to decide on treatments for breast cancer, EBV+ post-transplant lymphoproliferative disease, focal segmental glomerulosclerosis, presbyopia, and severe allergic reactions.
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 ...
Aurobindo Pharma has recently informed exchanges that the United States Food and Drug Administration (US FDA) completed an inspection of Unit-V, the API manufacturing facility of Apitoria Pharma ...
Moleculin Biotech, Inc., (Nasdaq: MBRX) ('Moleculin” or the 'Company”), a late-stage pharmaceutical company with a broad ...
Screenshot - Head of the Indonesian Food and Drug Authority (BPOM) Taruna Ikrar in Jakarta, Friday (November 28, 2025). ANTARA/HO-Badan Pengawas Obat dan Makanan Jakarta (ANTARA) - Indonesia's food ...
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