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Status Update- MDR Surprises and Key Regulatory Developments
Status Update- MDR Surprises and Key Regulatory Developments

Our Price: $395.00

Product Code: WB-7228

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About the Product
Includes 1 Hour and 30 Minute Windows Media Video File and PowerPoint presentations for immediate download.

The MDR is currently being translated into each of the official EU languages and is expected to enter into force in Q1 of 2017. Last minute political negotiations have resulted in a variety changes and interpretations that will have a significant impact on device manufacturers. These changes include the revision of the mandatory clinical evaluation consultation procedure, reclassification of clinical decision support software and amendments to the transition regime. In order to fully prepare for successful implementation and management of the regulation, manufacturers must have a better understanding of the most recent changes and how they apply to their organization.
  • Next steps in regulation approval- “Date of entry into force"
  • Real world timelines and application of transitional regime

Erik Vollebregt

Axon Lawyers

Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:
  • Regulatory Affairs
  • Legal Counsel
  • Compliance Officers

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