FDA Findings: Requirements For Calibration

The FDA enforces a number of strict requirements regarding the calibration and maintenance of equipment. Calibration is essential not only for meeting regulatory standards but also for improving accuracy, safety, and overall quality. It should be seen as more than just routine maintenance—it’s a proactive measure for continuous quality improvement. In this webinar, we will explore common calibration findings highlighted by the FDA and offer practical insights to help you better prepare for regulatory audits. You’ll discover how implementing a comprehensive calibration program can streamline processes, enhance compliance, and significantly reduce quality risks.

In this presentation, attendees will gain valuable knowledge on:

• Key FDA Calibration Findings: Understand common deficiencies and pitfalls that organizations often face during inspections and learn how to avoid them.
• Developing a Comprehensive Calibration Program: Learn how to design and implement a robust calibration program that aligns with both FDA requirements and industry best practices.
• Enhancing Process Accuracy and Safety: Discover strategies for optimizing equipment calibration to improve process reliability, safety, and product quality.
• Real-World Examples: Explore case studies and data-driven insights to inform your approach to calibration and ensure regulatory compliance.

This webinar will equip you with the tools and strategies needed to strengthen your calibration efforts and better position your organization for success in regulatory audits.