Webinar Registration

About the Webinar

With the publication of the NEW Medical Device Regulation (EU) 2017/745 on April 5th 2017, Obelis is happy to introduce a new Webinar presenting the key changes brought by the Medical Device Regulation – its definitions, critical timelines and conformity assessments.

The Webinar will touch upon the general requirements on Economic Operators, such as Authorized Representatives, Importers and Distributors in the European Union. Ultimately, the objective of the Webinar is provide all attendees a clear understanding of how this NEW Regulation will impact on their operations towards helping them create a NEW strategy for their CE Marking and European Market.

This webinar will not be a live session. You will receive the link the 1/02. But don’t worry you will have the ability to ask your questions anyway>

Speaker: Mr. Doram Elkayam – Chief Operations Officer (Obelis).