GMED North America’s Training Center

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.


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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.


Customized Courses

If you have a specific training need or want us to adapt training to focus on specific processes (i.e. pre-market requirement vs post-market requirements…) or targeted public (Management, QA/RA, R&D, auditors…), our staff can work with you to design a tailored course. Regardless of the type of training needed, rely now on GMED North America.

Request a customized course today!


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.

Training Catalog

European Medical Devices Regulation (EU) 2017/745

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Medical Device Electrical Safety – IEC 60601-1 3rd Edition (Ed3.1) and Introduction to Electromagnetic Compatibility (EMC) Requirements

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Medical Device Single Audit Program (MDSAP) for Manufacturers

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Post Market Surveillance and Vigilance New Requirements under the European Medical Device Regulations

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Risk management applied to Medical Devices (ISO 14971:2019)

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The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745

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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