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

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

Technical Documentation per (EU) Medical Device Regulation 2017/745 - 3 Half-Day Sessions; Online Training; October 14-16, 2025

By GMED North America, Inc.

Date and time

October 14 · 7am - October 16 · 11am PDT

Location

Online

Refund Policy

Refunds up to 7 days before event

About this event

  • Event lasts 2 days 4 hours

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.


Tags

Organized by

GMED North America, Inc.
Early bird discount
15% off applied
From $1,147.50