Medical Device Cybersecurity

Medical Device Cybersecurity
Medical Device Cybersecurity – How to start, with Axel Wirth Chief Security Strategist, MedCrypt

Cybersecurity risk management as a discipline is not new, however in these years cybersecurity for medical devices have more and more focus both due publicized real-life incidents and due to increased EU and FDA regulatory requirements.
As many new Medical Devices are connected to network, use cloud services, cybersecurity risk management needs to be part of standard engineering processes used to produce software-based medical devices.
Cybersecurity is not only needed for regulatory reasons, also to provide for patient safety and privacy and to protect a company's business interests. Cybersecurity requires new skills and processes for a Medical Device company and its engineers, yet many find it can be difficult to get started. 

In this Webinar you will get an introduction to cybersecurity for medical devices, cybersecurity process, and regulatory requirements – which you can you use as jump-off point for your endeavor to implement cybersecurity-capable engineering processes for your future Medical Devices.

The Webinar will be conducted by Axel Wirth, Chief Security Strategist at MedCrypt, Author of the book:  Medical Device Cybersecurity for Engineers and Manufacturers.
Axel has worked in cybersecurity with special focus on medical devices for many years and have a lot of real life as well as regulatory experience within the field.

 Agenda:

Introduction: 

  • What’s Cybersecurity about, short high-level intro
  • Cybersecurity in historical perspective 
  • Cybersecurity and medical devices

Why is cybersecurity important?

  • Incl. real life examples, showing impact of cybersecurity events on:
    Business
    Safety
    Privacy
    Regulatory

Cybersecurity best practices and processes

  • High level intro
  • Some detailed examples
  • Including cybersecurity in the product/software development lifecycle
  • Cybersecurity risk management introduction
  • Cybersecurity in relation to safety and privacy risk management

Regulatory requirements/expectation for Cybersecurity 

  • US FDA and IMDRF
  • EU MDR / MDCG

How to proceed

  • Literature and resources

Registration procedure for the webinar: Once you have registered you will receive a confirmation e-mail. At the bottom of this mail you will find a link to the webinar. You log in through this link and are forwarded to the site where the webinar is shown.

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Organizer: The Danish Society of Engineers, IDA

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Information
  • When

    20. jun. 2022 16:30 - 18:00
  • Where

    Webinar - In front of your pc/tablet/phone

  • Registration Deadline

    19. jun. 2022 - 23:59

  • Organizer

    IDA LifeScience

  • Available Seats

    153

  • Event Number

    345199