Attaining Your CE Mark for Your Medical Device in the EU 2020 Middletown United States
Attaining Your CE Mark for Your Medical Device in the EU 2020 Middletown United States
Attaining Your CE Mark for Your Medical Device in the EU 2020 Middletown United States
Why Should You Attend:
If you manufacture products for the EEA it is imperative that you know and understand the regulations that govern the CE marking process particularly in light of the new EU medical device regulation. Manufacturers, distributors, and importers all have roles to play and have responsibilities concerning CE marking.
If you are a manufacturer it is your responsibility to:
If you are a distributor you must check the presence of both the CE marking and the necessary supporting documentation.
If you are importing a product that is from a third country you have to check that the manufacturer outside the EU has undertaken the necessary steps. You must check that the documentation is available.
This webinar will begin with an understanding of the new EU Medical Device Regulation and will walk through the CE marking process explaining all relevant aspects of it to include acquiring and displaying the CE mark.
CE marking is required for many products. CE marks:
Learning Objectives:
At the completion of this webinar, participants will be able to:
Areas Covered in the Webinar:
Who Will Benefit:
Anyone involved in the manufacturer of medical devices for the EU market.
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