Nearly two dozen women across the nation have filed lawsuits against a pharmaceutical giant over a contraceptive linked to a debilitating bra ...

Sale Sharks brought a resounding end to Bristol Bears’ festivities with a thumping 38-0 victory on the road at Ashton Gate.

At the start of 2025, the vaping business in Kentucky could be taking a big hit. House Bill 11 also goes into effect on Jan. 1. Retailers will only be able to sell vape products that have received ...

The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's ...

The Macao IP Office has assigned number J/9010 to the patent with an entry date of December 17, 2024. Macao is a Special Administrative Region (SAR) of the People’s Republic of China which affords it ...

Opdivo is part of a class of drugs called PD-1 inhibitors, which enhance the immune system’s ability to fight cancer by ...

Tevimbra is also approved in the U.S. as monotherapy for the treatment of adult patients with unresectable or metastatic esophageal squamous cell carcinoma after prior systemic chemotherapy that doesn ...

The Food and Drug Administration is prohibiting the use of a red-capped psychedelic mushroom in foods like gummies and edibles. These products have grown in popularity, but they've also been linked to ...

Shilpa Medicare informed that it's Unit 4, Jadcherla, and Unit 7, Nacharam in Hyderabad, Telangana had undergone a GMP inspection by Ministry of Health, Belarus for GMP certification from the Eurasian ...

Both units of Shilpa Medicare (Unit IV and Unit VII), have now received GMP approval of Eurasia, the member countries for which are Belarus, Russia, Kazakhstan, Kyrgyzstan and Armenia.

The Food and Drug Administration is proposing a rule that cosmetic companies would have to take extra steps to ensure that ...

The U.S. Food and Drug Administration has approved the first generic version of Victoza (liraglutide injection), ...