Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Website https://www.complianceonline.com/medical-device-single-audit-program-mdsap-us-canada-brazil-australi |
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Deadline: October 08, 2019 | Date: October 08, 2019
Venue/Country: U.S.A
Updated: 2019-08-21 16:28:43 (GMT+9)
Call For Papers - CFP
This webinar will focus on the key regulatory requirements for medical devices for the participating MDSAP countries of U.S., Canada, Brazil, Australia and Japan. It will address key topics such as device classification, licensing pathways, medical device GMP, inspections, device labeling, license holder responsibilities and more.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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