GDPR & MDR for Medical Applications with Jovan Stevovic
GDPR is a well-known regulation now that is impacting all sectors as this helps to keep your data protected. So this also means that the Medical Device product should comply with it. But how to do that?
Jovan Stevovic is the CEO of Chino.io. He will help us to understand “What is GDPR?” and the link between GDPR and MDR 2017/745.
If your products are not compliant to GDPR, you can be heavily fined by the European member states so better understand it and put in place a strategy to protect the data of your customers or users.
But what are the elements to consider to be compliant to GDPR? and who should be on your project to support it and be sure that you are translating correctly the GDPR requirements to your design? This topic is really difficult as any miss can make your product not compliant. And the cost to be GDPR compliant can also be increased if you have not considered that from the beginning of your development.
Who is Jovan Stevovic?
Jovan Stevovic, Ph.D., is the co-founder and CEO of Chino.io, a platform that makes health applications GDPR and HIPAA compliant “out of the box”. Jovan has over a decade of experience in the health IT industry. He completed his Ph.D. at the University of Trento in 2014.
His research explored technologies and protocols to allow health data to be shared in a legally-compliant and secure manner. This work directly led to setting up Chino.io.
Currently, Chino.io helps companies in most EU states and the US to innovate in digital health.
- Jovan Stevovic Linkedin: https://www.linkedin.com/in/jovanstevovic/
- Chino Website: https://www.chino.io
- Episode 11 – Software validation: https://podcast.easymedicaldevice.com/11
- eBook about MDR and GDPR: https://www.chino.io/a/chino-io-ebook-medical-device-regulation-ehealth-applications
- eBook about GDPR: https://www.chino.io/a/chino-io-ebook-GDPR-compliance