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Technical Documentation per (EU) Medical Device Regulation 2017/745
By GMED North America, Inc.
Online event
Overview
Technical Documentation per (EU) Medical Device Regulation 2017/745 - 1.5-Days of Sessions; Online Training; March 3-4, 2025
Schedule (all times ET)
- Day 1: 9:00am - 5:00pm
- Day 2: 9:00am - 1:00pm
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.
Category: Science & Tech, Medicine
Good to know
Highlights
- 1 day 4 hours
- Online
Refund Policy
Refunds up to 14 days before event
Location
Online event
Organized by
GMED North America, Inc.
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