Cyber security compliance for the Healthcare Industry

webinar on Cyber Security Compliance for the Healthcare Industry

There are multiple regulatory, ethical and business reasons to ensure that all digital healthcare and medical devices are thoroughly tested and secure. Failing to ensure medical device cyber security could lead to significant reputational damage for device manufacturers and healthcare organisations that use insecure technology.

OUR WEBINAR WILL TACKLE THESE POINTS, FOCUSING ON:

• MDD versus MDR, differences and challenges between the two
• Introduction to MDCG (Medical Device Coordination Group) and its guidelines on cyber security
• Why Compliance with UL2900-2-1 and IEC/TR 60601-4-5?

HOW CAN TÜV SÜD HELP YOU?

TÜV SÜD is a world leader in cybersecurity testing and has worked with medical device manufacturers around the world to assess the quality and safety of their devices. We have extensive experience of conducting testing on a wide range of networked medical devices.

Our assessments are based on IEC 62443-4-2, UL-2900-2-1 (based on UL-2900-1), a TÜV SÜD internal checklist and the FDA guidance; thus aiding your compliance to regulations and access to global markets.

Our services and scope include:

• Concept assessment
• Compliance assessments
• Customised solutions
  
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