The FDA imposes several stringent requirements concerning the calibration and maintenance of equipment. Calibration plays a crucial role in enhancing accuracy, safety, and quality, and should be viewed as more than just a maintenance activity—it is a proactive step towards continuous quality improvement. In this webinar, we delve into common calibration findings reported by the FDA and provide practical insights to help you prepare for regulatory audits. You'll learn how implementing a robust calibration program can optimize processes and significantly reduce quality risks.
In this presentation, viewers can expect to learn:
- Key FDA calibration findings and common pitfalls to avoid.
- How to develop a comprehensive calibration program aligned with industry guidelines.
- Strategies for enhancing process accuracy and safety through effective calibration.
- Real-world examples and data to guide your approach to regulatory compliance.
Speakers:
Matt Thompson, Sr. Director, Pharma Services
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