Technical Documentation per (EU) Medical Device Regulation 2017/745

Schedule (all times ET)

• Day 1: 10:00am - 2:00pm
• Day 2: 10:00am - 2:00pm
• Day 3: 10:00am - 2:00pm

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 companies identify and understand the key elements required to establish their medical technical file as part of their CE marking application process.

For program and more information, click here.