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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

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

Speaker Interviews