An inter-ministerial committee formed by the Union health ministry has recommended amendments to the Food Safety and ... of certain items to the drug regulatory authority and bring in standards ...
Government investigations are an ever-present reality for companies operating in FDA-regulated industries. Whether you're in ...
The FDA has issued final guidance aimed at tattoo ink manufacturers, distributors, and packers on preventing microbial ...
The "FDA Regulatory Compliance for Drug and Biotech Product Training Course" training has been added to ResearchAndMarkets.com's offering. This course will benefit professionals involved in working ...
The Times of India on MSN4d
Granules India’s Unit V facility in Andhra Pradesh gets US FDA EIR with NAI statusPharma player Granules India Limited on Friday said it has received an Establishment Inspection Report (EIR) from the US Food ...
Biocon Biologics on Wednesday said its drug substance facility in Bengaluru has been classified as voluntary action indicated ...
Ethiqa XR now includes captive rodents and laboratory rabbits for 72-hour post-procedural pain management on its label ...
Biocon Biologics' Bengaluru unit classified as voluntary action indicated by US FDA: Our Bureau, Bengaluru Thursday, October 31, 2024, 12:15 Hrs [IST] Biocon Biologics said its dr ...
Chime Biologics and Waterstone Pharmaceuticals announce a strategic partnership to provide integrated services for t ...
Bengaluru: Biocon has announced that the U.S. Food and Drug Administration (USFDA) has classified Biocon Biologics' Drug ...
Drugmaker Granules India has received an establishment inspection report (EIR) from the U.S. Food and Drug Administration ... From April 8-12, the U.S. FDA had conducted a comprehensive pre-approval ...
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