Batch Record Review and Product Release

Description

This course shows how to review batch records the way regulators expect—practical, defensible, and inspection-ready—so product release decisions are confident, consistent, and audit-proof.

Why This Training Matters:

Batch record review isn’t paperwork. It’s the final gate between a compliant product and a regulatory nightmare. One missed entry, one unexplained correction, or one poorly trained reviewer can delay release, trigger deviations, or invite inspection findings you never saw coming. This webinar focuses on how batch records should be reviewed in real pharma, biologics, and medical device operations—not theory, not checklists copied from SOPs.

You’ll understand what regulators actually expect when they look at executed batch records, how reviewers should be trained and qualified, and how Quality and Production must work together without friction. We’ll break down what to look for line-by-line, how to handle discrepancies confidently, and how to document decisions that hold up during audits, investigations, and product release.