The United States Food & Drug Administration (FDA) did a routine Good Manufacturing Practice (GMP) inspection at Dr Reddy's ...

"At the end of the inspection, the agency issued a Form FDA 483 with one observation which is procedural in nature," it added ...

Torrent Pharmaceuticals announced that the United States Food and Drug Administration (USFDA) conducted a routine good manufacturing practices (GMP) inspection at its formulation manufacturing ...

The drug maker will respond to the USFDA within the prescribed timeframe and will work in close collaboration with it to ...

A previous report heard inexperienced officers were struggling to deal with a "tsunami of drugs" at category C HMP Hindley ...

Incidents related to drug use inside a low-security women's prison in Waseca prompted officials to initiate ...

FDA cites Granules, a large Indian generic drug manufacturer, for tossing truckloads of important documents from a facility ...

From truckloads of torn documents to avian incursions in the production plant, Granules India’s recent manufacturing ...

Ben Mosier, HIWU executive director, said at Tuesday’s news conference that the organization determined the UK lab ...

The FDA has issued a warning letter to Regenerative Processing Plant after conducting an inspection of the facility. The plant manufactures two ophthalmic drug products, Regener-Eyes Professional ...

Theratechnologies’ supply hiccup is the second caused by third-party manufacturing problems in less than a week. On Friday, ...

In its latest warning letter, FDA raised concern that the company was still producing eye drops with amniotic fluid, even ...