Have you ever wondered how to set up a packaging validation according to ISO 11607? Join us for a comprehensive webinar, “Packaging Validation 101,” designed to teach you the fundamentals of packaging validation. This session will cover essential topics such as determining an appropriate sample size for testing, writing a validation protocol, developing a test plan, selecting suitable tests, and considering family grouping and worst-case scenarios. Additionally, it will address the creation of appropriate samples for validation, ensuring that your packaging meets all necessary requirements.
ISO 11607 Part 2 focuses specifically on packaging process validation, and this webinar will delve deeply into basic validation concepts. You will learn how to define the validation process, establish seal acceptance criteria, and understand qualifications and routine process monitoring. The webinar will equip participants with a thorough understanding of the validation requirements outlined in ISO 11607 and provide practical guidance on how to implement these requirements effectively within their own organizations.
By attending this webinar, you will acquire the knowledge and skills necessary to ensure your packaging meets regulatory standards and provides adequate protection for your medical devices. The session is ideal for professionals involved in packaging design, quality assurance, and regulatory compliance. It is also beneficial for those who are new to packaging validation or looking to update their knowledge on the latest industry standards and practices.
This webinar will empower you to create robust packaging validation protocols that comply with ISO 11607, thereby enhancing the safety and effectiveness of your medical devices. With expert insights and practical advice, you will be well-prepared to tackle the challenges of packaging validation and ensure that your products are ready for the market. Don’t miss this opportunity to improve your understanding and implementation of packaging validation standards, ultimately leading to more reliable and compliant medical devices.