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MDCG 2019/16 Cybersecurity

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Understanding MDCG 2019/16 requirements

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.

main topics discussed:

  • Pre-Market Requirements

  • Post Market Requirements

  • Other Legislation and guidance’s (EU and international) relevant for cybersecurity of medical devices

About the speaker

Francisco Navarro Cybersecurity ExpertFrancisco Navarro

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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