Sterilization validation is a critical phase in the lifecycle of sterile products. This webinar will focus on the Performance Qualification (PQ) methods for Gamma irradiators, which are the final step before moving into routine sterilization. The webinar will review the purpose of PQ, reference standards used in the industry, and how to develop a PQ strategy that is both efficient and capable of consistently meeting product specifications.
Viewers will learn about the inputs and outputs of PQ, the importance of maintaining effectiveness in the sterilization process, and will gain insights through real-life examples to increase their knowledge. The session will cover various aspects of the PQ process, including the validation of equipment, processes, and materials to ensure they meet predefined standards.
The webinar will delve into the critical elements of PQ, such as dose mapping, dose auditing, and the calibration of dosimetry systems. It will highlight how to interpret and use data from these activities to refine and enhance the sterilization process. Additionally, the presentation will address common challenges encountered during PQ and provide practical solutions to overcome these hurdles.
By understanding the principles of PQ, professionals involved in quality assurance, sterilization, and product development can optimize their validation strategies. This knowledge will help them ensure that their sterilization processes are robust, compliant, and capable of delivering consistent results. Attendees will leave with a comprehensive understanding of how to execute an effective PQ, ensuring their products are reliably sterilized and meet all regulatory requirements.
This webinar is essential for anyone seeking to deepen their expertise in sterilization validation and improve the efficiency and reliability of their sterilization processes.