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MDR: Clinical evaluation requirements

MDR: Clinical evaluation requirements

After our MDR: Status & Highlights webinar, we are now zooming in on the Clinical Evaluation Requirements, one of the major changes in the Medical Device Regulations. This is the second broadcast in our series of three webinars, the "Expert Sessions MDR". Register now and secure your spot! 

On December 19, DEKRA’s MDR expert and Vice President of Team NB Guy Buijzen and internal clinical expert Dr. Pedro Eerdmans will address, amongst others:

•         Clinical evaluation

•         Post market surveillance and post market clinical follow-up 

•         CE mark obtained through equivalence 

The "Expert Sessions MDR" is a series of three webinars that sheds light on the most important aspects or developments around the new regulation. In the first session, broadcasted on October 23, we gave an update of the most important developments. After the coming webinar, the third session will follow on January 23, 2018 focusing on classification and conformity assessment routes.

We are looking forward to welcoming you! Please click the ‘Subscribe’ button to join us. Not able to watch live? Register and receive the link after the webinar to watch the on demand version. Please note that we will also organize various other webinars in 2018, starting with our IVDR webinar on February 15, 2018.

Register now and secure your spot! 

Tuesday

19

December 2017

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