The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Mar 12, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensuring compliance with Good ...
This article explores the US and EU compliance requirements to ensure patient safety for GMP ancillary materials in cell and gene therapy (CGT) manufacturing.
Both the USA cGMP 1 and EU GMP 2 dictate that cleanroom classification must be carried out according to ISO 14644-1. The version of this ISO standard released in 1999 4 was rewritten by a group of ...
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