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The NIS 2 Directive establishes new cybersecurity requirements for medical device manufacturers

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Published on: 10 January 2023
Published by a LexisNexis EU Law expert

Table of contents

  • Cybersecurity requirements for medical device and IVD manufacturers in the NIS 2 Directive
  • Next steps

Article summary

Life Sciences analysis: Elizabeth Anne Wright, partner, Alexander Wenzel, associate and, Anastasia Vernikoum, legal trainee of Cooley, discuss how the cybersecurity requirements established in the NIS 2 Directive apply to medical device manufacturers.

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Jurisdiction(s):
European Union

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