European Medical Device Regulation (EU) 2017/745
European Medical Devices Regulation (EU) 2017/745; 2-Days, Virtual Training; June 23-24, 2026.
Schedule (all times EST)
- Day 1: 9:00am - 5:00pm
- Day 2: 9:00am - 5:00pm
About the training
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (or EU MDR) – was published on May 5th, 2017 and entered into force on May 25th, 2017.
GMED North America has designed a comprehensive training course to help medical device industry companies get ready for their application to obtain and/or maintain CE marking for their product(s) and:
- Gain an understanding of the changes introduced by EU MDR requirements;
- Assess the impacts of those changes on their organizational and structural activities.
For program and more information, click here.
European Medical Devices Regulation (EU) 2017/745; 2-Days, Virtual Training; June 23-24, 2026.
Schedule (all times EST)
- Day 1: 9:00am - 5:00pm
- Day 2: 9:00am - 5:00pm
About the training
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (or EU MDR) – was published on May 5th, 2017 and entered into force on May 25th, 2017.
GMED North America has designed a comprehensive training course to help medical device industry companies get ready for their application to obtain and/or maintain CE marking for their product(s) and:
- Gain an understanding of the changes introduced by EU MDR requirements;
- Assess the impacts of those changes on their organizational and structural activities.
For program and more information, click here.
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Highlights
- 1 day 8 hours
- Online
Refund Policy