Our expertise enhancing your skills
As a professional in the medical device or in vitro diagnostic medical device industry, you want to develop the skills and knowledge you need to handle the challenges you’re facing.
Choose GMED North America’s Trainings
Established international organization
GMED is a notified body and an international certification body for products and quality management system in the medical device field.
Our experts’ experience and knowledge of the medical device industry allow us to offer a variety of training content adapted to the medical device manufacturers’ needs.
We focus on your challenges and provide attendees with a clear “take-home” value.
GMED’s trainings feature
- Hands-on practical case studies to encourage material retention & application;
- Qualified Trainers & Medical Device Experts for a gain of experience;
- In-house and/or public training scheduled for your convenience.
Limited number of attendees per session
The number of participants is maximized to fifteen to provide a stimulating and practical working environment.
We help you built-in knowledge checks that will allow you to apply and reinforce the mastery of new concepts explored throughout the training.
2023 training offer
Our wide range of virtual training courses will enable you to acquire the skills you need to implement European and international regulations and manage risks.
Download the 2023 training calendar by clicking on the icon, and book the course(s) that will enable you to meet the technical, regulatory, or normative challenges you are facing.
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
[NEW in 2023]
European Medical Devices Regulation (EU) 2017/745
ISO 13485:2016 Requirements
Medical Device Electrical Safety – A Review of IEC 60601-1/A2
Medical Device Single Audit Program (MDSAP) for Manufacturers
Post Market Surveillance and Vigilance New Requirements under the European Medical Device Regulations
Risk management applied to Medical Devices (ISO 14971:2019)
Technical Documentation per (EU) Medical Devices Regulation 2017/745
[NEW in 2023]
The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745
Request a training today
We offer a variety of training courses and focus on your challenges to provide our attendees with a clear “take-home” value