Uncovering GDP violations during audits is a crucial part of maintaining pharmaceutical quality standards. Yet, the list of discovered shortcomings can be extensive, posing significant challenges.
In this webinar recording you'll discover how to tackle these challenges, by:
- Identifying underlying issues to effectively manage and mitigate deviations, ensuring compliance and operational excellence.
- Understanding the criticality of detecting Out of Specification (OOS) results and applying Corrective and Preventive Actions (CAPA) to maintain product integrity and proactively address non-conformances.
- Discovering strategies for handling complaints, managing risks, conducting thorough audits to uncover GDP violations,
Learn more in this in-depth exploration of managing Quality Events for GDP. Simply fill in the form below to watch the webinar. Transform your compliance strategy today!
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