Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules

Date : 12th October 2017 to 13th October 2017

Place : Switzerland, Zurich, switzerland

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900986SEMINAR?allconferencealerts-October-2017-SEO

Contact Person:Eevnt Manager

Description:

Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules

Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules will be held in Zurich, switzerland,Switzerland on date 2017-10-13

---

Deadline for abstracts/proposals : 10th 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 in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by dev

Conference Highlights :Clinical Research Associates Clinical Project Managers Regulatory Affairs Professionals Clinical Investigators and Clinical Research Regulatory Affairs Management Regulatory Affairs Specialists

Venue :Zürich, Switzerland

Check the event website for more details.