This website uses cookies. For more information please contact us or consult our privacy policy.

Your binder contains too many pages, the maximum is 40.

We are unable to add this page to your binder, please try again later.

This page has been added to your binder.

Key issues of the new EU Medical Devices Regulation – Classification, Conformity Assessment and Clinical Evaluation

October 6, 2016, 12. Augsburger Forum für Medizinprodukterecht, Augsburg

Share this article: