Course Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations) has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Classification systems differ from that of the United States or European Union in select countries Medical devices are classified depending on their risk leve

Date : 2nd November 2017 to 3rd November 2017

Place : Switzerland, zurich

Website :https://www.eventbrite.com/e/medical-device-registration-and-approval-process-for-the-pacific-rim-ntz-tickets-32333062059?aff=NDT

Contact Person:Paula Edwards

Description:

Course "Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Classification systems differ from that of the United States or European Union in select countries Medical devices are classified depending on their risk leve

Course Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations) has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Classification systems differ from that of the United States or European Union in select countries Medical devices are classified depending on their risk leve will be held in zurich,Switzerland on date 2017-11-03

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Deadline for abstracts/proposals : 28th October 2017

Keynote Speakers : David R. Dills, Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience

Conference Highlights :This seminar will provide an overview and in-depth snapshot of the medical device registration and approval process for Asia Pacific and with the corresponding regulatory authorities. Employees who will benefit include all levels of management and departmental representatives from key functional areas and those who desire a better understanding or a "refresh" overview of the medical device registration process

Venue :8152 Opfikon, Switzerland

Check the event website for more details.