Course Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Date : 16th October 2017 to 17th October 2017

Place : Singapore, Orchard

Website :https://www.eventbrite.com/e/japan-regulatory-filing-requirements-and-compliance-processes-for-medical-devices-ntz-tickets-32332688943?aff=NDT

Contact Person:Paula Edwards

Description:

Course "Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Course Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. will be held in Orchard,Singapore on date 2017-10-17

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Deadline for abstracts/proposals : 5th 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 Japan. 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, including: Clinical Research Associates Clinical Project Managers

Venue :Singapore 238867

Check the event website for more details.