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 ...

A team comprising lead experts from WHO's headquarters in Geneva, India office, and drug regulators from other nations ...

A drug production facility in Durham run by a Chinese company violated multiple safety regulations, according to the FDA. A ...

The move comes after a string of Indian-made drugs in regions as far afield as North America, Africa and Central Asia were ...

Dr. Reddy's Laboratories announced that the U.S. Food & Drug Administration (FDA) completed a routine Good Manufacturing ...

A police officer's drug dealing was discovered after he accidentally dropped a bag of cocaine at his daughter's primary ...

South Korean drug maker Daewoong Pharmaceutical has announced the launch of a new stem cell plant in Indonesia, marking the ...

Dr. Reddy's Hyderabad R&D centre passes USFDA inspection with zero observations, ensuring compliance with GMP standards.

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

Andrew Talbot admits stealing and accessing GMP's computer system illicitly but denies supplying drugs and misconduct in ...

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