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Introduction

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.

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Venue

Online Event

Online Event, 161| Mission Falls Lane| Suite 216, Fremont| CA 94539, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, United States, Fremont, 94539, United States of America
1800 447 9407
Contact us by email

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