Digital health compliance, made simple MDR and eHealth - free eBook |

Free eBook: How to build MDR certified eHealth applications

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 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.

See how saves you time, money and reduces risk.

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Jovan Stevovic, CEO of

About the Author

Jovan Stevovic

Dr Jovan Stevovic is the co-founder and CEO of Jovan has over a decade of experience in the eHealth industry. He is an active member of the eHealth startup community in Berlin and Italy. He is an expert in data security for eHealth and has a PhD in this field.

Marion Lepmets, CEO of SoftComply

About the Author

Marion Lepmets

Dr Marion Lepmets is the CEO and co-founder of SoftComply. She has an extensive academic background in medical device software development, she has been a member of international standards working groups and has co-authored IEC TR 80002-3.