Our experts explain why MDR matters for eHealth, how to build compliant applications and what tools you can use
From May 2020, many eHealth applications will have to comply with the Medical Device Regulation (MDR).
Our guide explains about MDR and the link with GDPR, the importance of ISO 13485, the MDR certification process, some technologies you can use and finishes by showing how using Chino.io speeds up the certification process for you.
✅ Learn about MDR and why it matters for eHealth.
✅ Understand the requirements for MDR-certified applications.
✅ Compare the pros and cons of different technologies.
✅ Find out why ISO 13485 is so important.