Reprocessing Validations for Medical Devices

Reprocessing Best Practices Webinar

View On-Demand Webinar

View On-Demand Webinar

In this enlightening webinar, we delve deep into the world of reprocessing, uncovering the nuances of current standards, particularly the recent ST98 rollout. Our expert-led discussion will not only guide you through the complexities of these standards but also offer you a platform to explore innovative practices reshaping the reprocessing landscape.

What You Will Learn:

  • Understanding ST98 and Its Industry Impact: Grasp the essence of the latest standards and their implications for manufacturers.
  • Insights from Industry Leaders: Gain valuable perspectives through a fireside chat-style discussion with renowned experts in the field.
  • Interactive Q&A Sessions: Have your specific queries addressed. This segment includes questions pre-submitted by you, our audience, ensuring a tailored and relevant discussion.
  • Best Practices & Practical Solutions: Discover actionable strategies and best practices that can be implemented in your operations.

Who Should Attend:

This webinar is ideal for professionals involved in medical device manufacturing, healthcare reprocessing, quality assurance, regulatory compliance, and anyone interested in understanding the latest trends and practices in reprocessing.

About the speaker

Christine Laube, Medical Product Expert and Biological/Analytical Testing Specialist at TÜV SÜD

Christine Laube, Technical Advisor

Christine Laube has more than 14 years of experience in microbiology testing and the medical device industry. In her current role as Technical Advisor at TÜV SÜD, Christine is responsible for technical documentation review of MDR submissions and facilitating biological and chemical testing services.

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