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In the next installment of our Cybersecurity in the Healthcare Industry series, we are covering MDCG 2019/16 and how to fulfill requirements of Annex I to the MDR with regard to cybersecurity.
Post Market Requirements
Other Legislation and guidance’s (EU and international) relevant for cybersecurity of medical devices
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