Webinar: Reprocessing validations for reusable medical devices

Watch the webinar on reprocessing validations for reusable medical devices and key requirements for safe, effective reuse.

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

Moderator

Christine Laube

Technical Advisor, TÜV SÜD

Christine Laube is a microbiologist and cell biologist with more than 20 years of experience in medical device, antimicrobial, and pharmaceutical testing. Her work focuses on biological safety testing, biocompatibility, chemical characterization, and regulatory strategy, helping manufacturers navigate complex safety assessment and compliance requirements throughout the product development process.