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.

The Data Protection Officer (DPO), is a corporate figure introduced by the General Data Protection Regulation GDPR, the EU's new law on Data Protection and Privacy matters.

Anonymisation and pseudonymisation are two key concepts for the General Data Protection Regulation (GDPR). The GDPR provides exceptions to many of the most burdensome provisions of the regulation when steps are taken to de-identify personal data using anoymisation or pseudonymisation.

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.

If data is in any way identifiable or can be connected to the user (directly or indirectly), the data collection process cannot make the claim of being anonymous.

GDPR fines are starting to bite. Find out about 3 of the most recent rulings from across Europe. Then read the 7 most important lessons the fines teach us.

As 2018 goes to the end, we reflect on our accomplishments. Now we are the only ISO 13485 certified Database as a Service (DBaaS) for Medical Data. Meaning that our customers cut time to market, costs, and eliminate risks related to health sensitive data management.