Amsbio, in collaboration with Nordmark Biochemicals, has broadened access to high-purity collagenase and neutral protease ...

CPHI China has long been recognized as a premier platform for connecting the entire pharmaceutical supply chain, from active ...

The inspection, conducted by Brazilian regulatory authority ANVISA, was held between June 30 and July 4. Earlier, it had ...

In parallel, the Company is expanding annual international cultivation capacity at its EU GMP-certified facility in Napanee, Ontario (the “Napanee Facility”) by approximately 30% in 2025.

MediPharm’s investment in expanding cultivation capacity by approximately 30% at its EU GMP-certified Napanee facility enhances the Company’s ability to meet growing international demand for ...

Dublin, June 04, 2025 (GLOBE NEWSWIRE) -- The New EU (European Union) GMP (Good Manufacturing Practice) Annex 1: Compliant Aseptic Operations Traini ...

Shilpa Medicare Ltd on May 6, 2025 issued a statement that it has been awarded the Good Manufacturing Practice (GMP) certificate by the European Medicines Agency (EMA) for Unit VI manufacturing ...

US 21 CFR 211 describes GMP for finished pharmaceuticals in the US. To find the equivalent regulations in the EU, it is easiest to go to EudraLex–Volume 4–Good Manufacturing Practice (GMP) guidelines ...

In August 2022, the European Union revised its guidelines for sterile medicinal products for human and veterinary use. These guidelines came into effect on August 25, 2023. West has compiled the most ...