MDR Training Academy
A unique medical device regulatory support platform that will accelerate your EU MDR transition
The complete medical device risk management program
Become ISO 13485:2016 compliant through dedicated training & resources
All you need to produce an MDR-compliant PMS systems for your entire device portfolio
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:
- Sign up and begin learning immediately through detailed videos, seminars and downloads.
- Build systems for your devices in lock-step with course progress using document templates and resources.
- Verify compliance through direct support, Q&A sessions and community engagement.
- Access powerful document management software for version control, archiving, training and regulatory audit.
- 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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