The U.S. Food and Drug Administration has lifted a clinical hold on three cell therapies being developed by CARsgen ...

Government investigations are an ever-present reality for companies operating in FDA-regulated industries. Whether you're in ...

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 FDA has issued final guidance aimed at tattoo ink manufacturers, distributors, and packers on preventing microbial ...

Athira Pharma, Inc. (ATHA) has disclosed a new risk, in the Regulation category. Athira Pharma, Inc. faces significant ...

The additional recruitments will help the Drugs Controller General of India enforce good manufacturing practices for ...

the US FDA has determined that the inspection has been classified as ‘No Action Indicated’ (NAI) without any Form 483 ...

This was a drug induced violent and sustained assault on a lady who was completely innocent. “Whatever sentence was imposed ...

The U.S. FDA inspection classified the facility as ‘No Action Indicated’ (NAI), indicating compliance with current good manufacturing practices (cGMP) standards and confirming no further regulatory ...

Venus Remedies’ Baddi robotic pre-filled syringe facility receives Malaysian PIC/S GMP approval: Our Bureau, Mumbai Tuesday, November 5, 2024, 12:15 Hrs [IST] Venus Remedies Lim ...

Pharma player Granules India Limited on Friday said it has received an Establishment Inspection Report (EIR) from the US Food ...

A suspected drug dealer was arrested after six people were injured in a hit-and-run horror on Bonfire Night. Emergency ...