MDR

The MDR (Medical Device Regulation) will be enforced from May 2020. Throughout the past year we received number of questions from digital health innovators on how it will affect their project development timeline.

The MDR will be enforced from May 2020. To help companies prepare for it, the EU has published a step-by-step implementation plan. Here we explain how the 12 step plan applies to eHealth companies.

Come and visit Chino.io at DMEA! The all-new DMEA conference runs from 9-11 April, 2019 at the Berlin Exhibition Grounds. Chino.io will be attending as part of the Berlin Partner stand D-103 in hall 3.2.

The new Medical Device Regulation promotes many eHealth apps to Class II or even Class III medical devices. Use our useful infographic to find out what MDR class your app is.

MDR will have a big impact on the eHealth market. Suddenly, software is being treated as a medical device. Here we look at how MDR affects your choice of cloud provider.

The new MDR becomes mandatory from 2020. Many eHealth applications will now be classed as medical devices. Here we discuss how MDR is related to GDPR and how they impact application development.

The motivations behind MDR and its impact on the EU eHealth market We look in more detail at the background to the new MDR. Read on to find out if MDR will be an innovation killer or lifesaver!