The Medical Device Coordination Group (MDCG) has released a guide on cybersecurity. The primary purpose of the guide is to provide medical device manufacturers guidance on how to meet the applicable essential requirements of the MDR and IVDR with regard to cybersecurity.
We will be conducting a webinar series on the topic of EU Cybersecurity Compliance for the Healthcare Industry.
Post Market Requirements
Cyber Security Expert for Medical Devices, TÜV SÜD
Before joining TÜV SÜD, Francisco Navarro gained more than 5 and half years’ experience working as Product Manager for a Medical Company, which had successful rollout of products (IaaS & SaaS) in more than 15 European countries and USA, responsible for regulatory requirements for go to market including GDPR compliance and Cybersecurity.
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Bosnia and Herzegovina