MDR Training Academy

A unique medical device regulatory support platform that will accelerate your EU MDR transition


  • Risk Management

    The complete medical device risk management program

  • Quality Management

    Become ISO 13485:2016 compliant through dedicated training & resources

  • Post-Market Surveillance

    All you need to produce an MDR-compliant PMS systems for your entire device portfolio

  • Document Management

    Powerful document management platform integrates your Risk Management, QMS & PMS files

A revolution in medical device regulatory support

Unlike any other service, our MDR Training Academy is designed to empower you and your team to build crucial regulatory systems and processes in-house, saving you time and money.

How it works

Our Academy is the complete solution to your medical device regulatory transition:

  1. Start learning immediately through detailed videos, seminars and downloads.
  2. Build systems for your devices in lock-step with course progress using document templates and resources.
  3. Verify compliance through direct support, Q&A sessions and community engagement.
  4. Access powerful document management software for version control, archiving, training and regulatory audit.
  5. All this and more for a single monthly fee with no up-front charges.

Want to learn more?

Please contact us to learn more about our Academy.

Stay informed

The first modules of our Academy will be launching in March 2022. Please complete the following form to be notified of updates and launch date announcements.

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