MEDDEV 2.7.1 Rev. 4 webinar in the top 5 of popular Medical Devices Webinars

December 20, 2016

The webinar "Understanding the Changes in MEDDEV 2.7.1. REV 4"  by Keith Morel, VP of Regulatory Compliance at Qserve Group is in the top 5 of most popular free Medical Device Webinars of 2016 at Greenlight.guru.

The new MEDDEV is both more instructive, and more prescriptive in particular regarding the use of evidence from equivalent devices. So what exactly are the implications of all these changes for device manufactures? How does this affect your CERs? are learnings from this webinar.

The On-Demand Webinar is still available:Clinical Evaluation in the EU for Medical Devices.

If you want to learn more about the new EU MDR and the consequences for your business? check our flyer "The roadmap to EU-MDR Implementation" or join our Modular European MDR workshop program.

 

 

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