Ongoing issues at Sun Pharma’s production facility in Gujarat, India, have resulted in the FDA putting the facility on import ...

Sun Pharmaceutical Industries Ltd (Sun Pharma) has confirmed that the US Food and Drug Administration (FDA) has classified ...

The PDA Regulatory Conference convenes more than 30 FDA experts to discuss cGMP excellence, compliance trends, and regulatory outlook, offering crucial insights for pharma manufacturing professionals.

The US FDA has classified Sun Pharma's Halol facility as "Official Action Indicated" after a June inspection, keeping the ...

Cohance Lifesciences announced that the United States Food and Drug Administration has successfully completed a current good manufacturing practices (cGMP) inspection at the its API manufacturing ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...

The U.S. Food and Drug Administration has issued a recall on deodorant sold online and at several major retail chains countrywide. In total, over 67,000 cases of three different types of deodorant ...

SHELTON, CONNECTICUT / ACCESS Newswire / September 9, 2025 / NanoViricides, Inc. (NYSE American:NNVC ) (the “Company”), a ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ...

The U.S. Food and Drug Administration (FDA) has designated a recall of multiple sunscreen products as Class II, the second highest of its three risk categories. The affected products included popular ...