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Free Webinar: Actors and their Duties in the European Medical Devices Regulation Revision

The new Regulation Draft details duties for manufacturers, distributors, and importers; as well as heightened duties for Competent Authorities, Notified Bodies, and the European Commission. Most of the actors will see their responsibilities modified if revisions to the medical devices regulatory scheme are approved, and will therefore need to be informed and prepared.

To present the main changes in responsibilities, as defined in the Regulation modification proposal, LNE/G-MED will host a free webinar, Actors and their Duties in the European Medical Devices Regulation Revision on Wednesday, February 13 at 2:00PM EST. Join us to hear how you may be affected by the Revision – Register now.

  • Who: LNE/G-MED North America
  • What: Actors and their Duties in the European Medical Devices Regulation Revision
  • When: Wednesday, February 13 at 2:00PM EST
  • Cost: Free
Contact LNE/G-MED - Your Global Quality Partner - Gain access to Europe, Canada & other World markets with CE Marking, ISO 13485 & ISO 13485 under CMDCAS

LNE/G-MED - Your Global Quality Partner - Gain access to Europe, Canada & other World markets with CE Marking, ISO 13485 & ISO 13485 under CMDCAS