Calibration plays a critical role in pharmaceutical engineering, directly impacting safety and quality compliance. Due to the emphasis placed on calibration during audits, companies often resort to over-calibration to ensure the reliability of their systems. While this approach prioritizes caution, it can lead to unnecessary resource expenditures without delivering proportional value. To enhance efficiency, it is crucial to analyze calibration processes, identify potential risks, and optimize calibration intervals. This must be done within a robust strategy that can withstand regulatory scrutiny while safeguarding product quality. In this session, you will learn how to:

• Achieve an optimal balance between resource allocation and maintaining process quality.
• Evaluate and assess the effectiveness of the calibration process.
• Implement strategies to optimize calibration intervals while ensuring high standards of safety.
• Analyze trends to identify opportunities for improving process efficiency and quality.
• Maintain compliance with GMP and uphold rigorous quality and safety standards.