The Medical Device Classification webinar explains the classification system in the US, the EU, following the Medial Device Directive (MDD), and the Canadian Medical Device Regulations (CMDR), and the guidance from the Global Harmonization Task Force (GHTF). This is a risk based approach implemented by regulatory authorities.
Medical Device Classification - US and the EU as per MDD, CMDR and GHTF - Webinar by GlobalCompliancePanel
12 February 2014, Fremont, United States
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Online Event, 161| Mission Falls Lane| Suite 216, Fremont| CA 94539, Fremont, 94539, United States
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