The performance of periodic sterilization dose audits is required when a sterilization dose has been established using Method 1, Method 2, or Method VDmax. This webinar will focus on the purpose and activities associated with such audits to demonstrate the continued effectiveness of the established sterilization dose.
Viewers will gain a greater understanding of the necessity of sterilization dose audits and the steps involved in conducting these audits. The webinar will provide comprehensive guidance on the regulatory requirements and best practices for performing sterilization dose audits, particularly for medical devices validated using the ANSI/AAMI/ISO 11137 standards.
The session will cover the critical aspects of dose audits, including the selection of appropriate audit methods, preparation for audits, and the interpretation of audit results. Viewers will learn about the various challenges and considerations involved in conducting dose audits for different types of medical devices. Whether you are new to dose audits or looking to enhance your current practices, this webinar will equip you with the tools and knowledge needed to ensure your sterilization processes remain effective and compliant.