CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of the MDR for Europe

Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland

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Event Details

Begins: November 29, 2018

End: November 30, 2018

Event Location: Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland

Website: https://www.global..64SEMINAR

Event Organizer

Event Organizer: Global Compliance Panel

Contact Person: John Robinson

Phone Number: 1-510-584-9661

Website: https://www.globalcompliancepanel.com/

Overview

Course "CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of the MDR for Europe" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

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