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Sterilisation & Reprocessing of Medical Devices

The latest advice on sterilisation and reprocessing: Guidance, methods & process development

Highlights Include:

Your Dedicated Update On Sterilisation And Reprocessing…
  • Evaluate the impact of the EU MDR & new ISO standards
  • Hear the latest on new EU legislation planned for reprocessing single use devices
  • Gain practical guidance on regulatory expectations for reprocessing devices
  • Stay up-to-date on standards for bioburden testing, environmental monitoring and bacterial Endotoxin
  • Bridge regulatory gaps to meet packaging validation standards EN ISO 11607

Hear Competent Authority, Notified Body and industry perspectives:
  • The Dutch National Institute for Public Health and the Environment (RIVM),
  • TÜV SÜD Product Service GmbH
  • Society for Sterility Assurance Professionals (SfSAP)
  • Cook Medical
  • BD Medical
  • Zimmer Biomet

Benchmark Your Processes And Take Away New Approaches With Industry Case Studies On:
  • Lifecycle Management of Reusable Medical Devices: Reprocessing Validation
  • Optimisation of the Ethylene Oxide (EO) Sterilisation Process
  • Reducing Ethylene Oxide (EO) Residue Levels and Compliance to ISO 10993-7
  • Gamma Sterilisation Validation and Monitoring
  • Evaluating the Interaction between Sterilisation, Packaging and Biocompatibility

Free On-Demand Content

Webinars. Webinars. Webinars.

Latest status and practical experience of implementing the new EU MDR

Bassil Akra, Vice President, Global Focus Teams (Cardiovascular, Orthopeadic and Clinical), TÜV SÜD Product Service GmbH, Germany

Speaker Interviews