MDR Training Academy

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

Overview

  • 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 MDR Training 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.

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