European in Vitro Diagnostic Devices Regulation (EU) 2017/746

Schedule (all times EST)

Day 1: 9:00am - 5:00pm

Day 2: 9:00am - 5:00pm

About the training

The European Union Medical In Vitro Diagnostic Device Regulation - IVDR EU 2017/746 – entered into force on May 26th, 2017. GMED North America has designed a comprehensive training course to help companies get ready for their application to obtain and/or maintain CE marking for their in vitro diagnostic device product(s) and:

• Gain an understanding of the changes introduced by European In Vitro Diagnostic Device Regulation – IVDR EU 2017/746;
• Assess the impacts of those changes on their organizational and structural activities.

For program and more information, click here.

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