Reprocessing Validations for Reusable Medical Devices

Reprocessing Validations: The Fundamentals, Challenges, and the Lifetime

Reprocessing validations are essential to ensure that medical devices are safe for the intended use and reuse. Manufacturers must ensure that their products are clean and sterile before it becomes available in a healthcare setting.

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This webinar will cover:

• Importance of reprocessing validations for reusable medical devices
• The requirements for cleaning, disinfection, and sterilization
• The methods used that are considered state of the art for each test type
• Considerations and common challenges
• Discussion on how the lifetime use of the device is impacted

About the Speaker

Christine Laube

Christine Laube has over 14 years of experience in microbiology testing and the medical device industry. In her current role as Medical Product Expert and Biological/Analytical Testing Specialist at TÜV SÜD, Christine is responsible for technical documentation review of MDR submissions and facilitating biological and chemical testing services.