Shares of Cipla declined 4% on January 7 after the US Food and Drug Administration (FDA) disclosed inspection observations ...

The U.S. Food and Drug Administration said on Tuesday that it will limit regulation of wearable devices and software designed ...

Takeda & Protagonist submit NDA to US FDA seeking approval for rusfertide to treat polycythemia vera: Osaka, Japan Wednesday, January 7, 2026, 17:00 Hrs [IST] Takeda, focused on c ...

US FDA accepts for priority review for Sanofi’s sBLA for Tzield for young children with stage 2 type 1 diabetes: Paris Tuesday, January 6, 2026, 12:00 Hrs [IST] The US Food and ...

The U.S. Food and Drug Administration has approved Omeros' drug for a dangerous transplant complication in adults and ...

In a major medical breakthrough, the US FDA has approved a new oral drug for Thalassemia, offering hope for a ...

CHENNAI: In a move to strengthen oversight and improve the safety of products reaching American consumers, the US Food and Drug Administration (FDA) has on Tuesday announced that it will increase ...

Dec 30 (Reuters) - Vanda Pharmaceuticals said on ‌Tuesday ​its drug for the ‌prevention of motion-induced vomiting was ...

WASHINGTON (Reuters) -The Food and Drug Administration is suspending a quality control program for testing of fluid milk and other dairy products due to reduced capacity in its food safety and ...

The Danish American who doubted Covid shots is meant to lead drug regulation – but has focused on vaccines ...

The FDA has granted breakthrough therapy designation (BTD) to sevabertinib (Hyrnuo, formerly BAY 2927088) for the first-line ...