Mastering Medical Device Reprocessing: Regulatory Expectations, Validation and Practical Solutions
Speakers:
- Kristin Rödig, Eurofins Medical Device Consulting Germany
- Dr. Stefan Holzmayr, Eurofins Medical Device Testing Microbiology
- Jessica Jankowski, Eurofins Medical Device Testing Microbiology
- Sophia Beck, Eurofins Sterile Packaging
- Dr. Laura-Marie Ammer, Eurofins Sterile Packaging
Date: 6th October 2026
Time: 09:00 - 16:45 CET
Gain practical insights into the regulatory and scientific requirements for the reprocessing and validation of reusable medical devices.
Learn how to navigate European and FDA expectations, avoid common validation pitfalls, and develop robust cleaning, disinfection, and sterilisation strategies through real-world case studies, expert presentations, laboratory insights, and interactive discussions.
📌 In this webinar, you will learn:
- European and FDA regulatory requirements, including ISO 17664 and ISO 10993
- Reprocessing validation for reusable medical devicesCleaning, disinfection, sterilisation, and lifecycle evaluation
- Developing compliant reprocessing strategies and addressing validation challenges
- Laboratory testing, sample preparation, and test execution
- Practical insights through case studies and expert discussions
👤 Who Should Join?
- Medical Device Manufacturers
- Regulatory Affairs Professionals
- Quality Assurance and Compliance Managers
- R&D and Product Development Teams
- Validation and Reprocessing Specialists
- Sterilisation and Microbiology Experts
- Technical and Clinical Affairs Professionals
- Anyone involved in the design, validation, regulatory submission, or lifecycle management of reusable medical devices
In Summary:
This on-site workshop provides a comprehensive journey through the regulatory and practical aspects of medical device reprocessing and reprocessing validation. Participants will be guided through current European and FDA requirements, including key standards such as ISO 17664 and ISO 10993, while gaining valuable insights into cleaning, disinfection, sterilisation, and lifecycle evaluation of reusable medical devices.