Technical Documentation per Regulation (EU) 2017/746 (IVDR)

Schedule (all times EST)

• Day 1: 9:00am - 5:00pm
• Day 2: 9:00am - 1:00pm

About the training

The European Union Medical In Vitro Diagnostic Device Regulation– Regulation (EU) 2017/746 (or EU IVDR) – 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 medical in vitro diagnostic device product(s) and:

• Gain an understanding of the changes introduced by EU IVDR requirements;

• Assess the impacts of those changes on their organizational and structural activities

For program and more information, click here.