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The Complete Guide to Batch Release in Manufacturing
In a highly regulated pharmaceutical environment, batch record review is one of the most time-consuming steps between production and patient. This guide covers everything quality and manufacturing teams need to know, from understanding the review process to implementing AI-powered Release by Exception.
Learn about:
- •What batch release is and why it matters in regulated industries
- •Common bottlenecks and risks in manual batch review processes
- •How MES digitises and automates batch record collection
- •Electronic Batch Records (eBR) and GMP compliance
- •Review by Exception: faster release without compromising quality
- •Integration with ERP and LIMS for end-to-end traceability
- •KPIs to measure and improve your batch release cycle time
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