Canadian Medical Device Regulations Web-based Seminars
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From GlobalCompliancePanel
Medical Device Classification - Webinar by GlobalCompliancePanel
... using the MDD version in effect after March 2010.
The Canadian Medical Device Regulations (CMDR) classifies devices into four risk categories (I, II, III, and IV). Classification follows a rule based system set forth in Schedule 1 of the CMDR.
The Global Harmonization Task Force (GHTF) has a guidance document on medical device risk classification that uses four classes (A, B, C, and D)
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