The plaintiff, Skylar Williams, accused Galderma Laboratories of producing a skin-care line that contains benzene. In one of ...
Dr. Reddy's Laboratories announced that the U.S. Food & Drug Administration (FDA) completed a routine Good Manufacturing ...
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 drug production facility in Durham run by a Chinese company violated multiple safety regulations, according to the FDA. A ...
In its latest warning letter, FDA raised concern that the company was still producing eye drops with amniotic fluid, even ...
Kerassentials is a novel formula designed to combat antifungal resistance and alleviate toenail itching. The formula h ...
The Food and Drug Administration sends warning letters to entities under its jurisdiction as part of its enforcement ...
The US Food and Drug Administration (USFDA) has issued a warning letter to Zydus Lifesciences for significant violations of good manufacturing practices at their Gujarat facility. The letter points ...
On August 8, 2024, the US Food and Drug Administration (FDA) partially revised the availability of certain glucagon-like peptide 1 (GLP-1) ...
Dr. Reddy's Hyderabad R&D centre passes USFDA inspection with zero observations, ensuring compliance with GMP standards.
South Korean drug maker Daewoong Pharmaceutical has announced the launch of a new stem cell plant in Indonesia, marking the ...