EU and US Drug Product Batch Records Review Webinar 2022 – ResearchAndMarkets.com
DUBLIN–(BUSINESS WIRE)–The “Reviewing Drug Product Batch Records” webinar has been added to ResearchAndMarkets.com’s offering. Batch record review is a GMP requirement. Furthermore, trending of manufacturing data facilitates continuous product improvement, which is the focus of a pending ICH guidance document (ICH Q12). Pharmaceutical manufacturers will be expected to demonstrate that their manufacturing processes continue to … [Read more…]