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Cyber Security for Medical Devices Training Course: live webinar

5-6 Nov 2020

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Cyber security and privacy is a domain where threats and regulations are quickly evolving. That includes the risks and compliance requirements in healthcare IT.

During this two-day intensive you will:

  • Get an overview of the regulatory and market challenges in European healthcare IT.
  • Learn how to integrate the GDPR, the NIS Directive and the MDR security and privacy requirements.
  • Explore the pros and cons of possible solutions, standards, frameworks and certifications.
  • Have interactive discussions about how your own challenges have been or should be addressed.

Who should attend?

  • Security, Privacy and Risk Managers and Architects
  • R&D, Product and Project Managers
  • Regulatory Affairs Managers
  • Healthcare IT Consultants and Auditors


Cyber Security and Data Protection: context and challenges for Healthcare IT providers

  • Regulatory versus market expectations
  • Direct and indirect requirements and risks
  • Relationship with best practice

Regulations Deep Dive

  • Requirements from the GDPR
  • Requirements from the NIS Directive
  • Cyber Security and Data Protection requirements from the MDR

Common customer requirements

Interactive discussion

Putting it all together

Solutions: useful frameworks and standards

  • Raison d'être, misconceptions
  • Which requirements do they help you meet?

The case for certification

  • Why?
  • Which certification scheme(s)?
  • Making the business case.
  • Adding new standards and schemes.

The case for more market standardisation

  • Challenges.
  • Existing initiatives.
  • Emerging initiatives

Interactive discussion

Book now

Book now

  attend Live webinar
5-6 Nov 2020
Live webinar
5-6 Nov 2020
Live webinar
GBP 1,099.00
EUR 1,579.00
USD 1,786.00
Until 24 Sep*
Online registration unavailable: this date is nearing full capacity; please call us on 020 7749 4730 to register.

Learn more about our different live training formats.

* Note the early booking discount cannot be combined with any other offers or promotional code

Customised in-house training

We can customise this course to meet the requirements of your organisation and deliver it at your location and/or online.

Contact us

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Previous customers include...

  • Advanex Europe Ltd
  • Astellas Pharma Europe BV
  • Bayer AG
  • Becton Dickinson
  • Biocorp
  • Biogen
  • Cantab Innovations
  • Chiesi Farmaceutici S.p.a.
  • Chiesi Farmaceutici SPA
  • Cochlear Ltd
  • ConvaTec LTD
  • DCA Design International
  • Flextronics Medical
  • Gerresheimer Regensburg GmbH
  • GSK
  • Haselmeier AG
  • Medicines and Healthcare Products Regulatory Agency (MHRA)
  • Nemera La Verpillière
  • Noble International
  • Nokia
  • Nordic Semiconductor
  • PA Consulting
  • Pfizer
  • Presspart
  • RB Healthcare UK
  • Sagentia Limited
  • SHL Group
  • Team Consulting Ltd
  • Weidmann Medical Technology AG

Good overall overview

Frederic Bustos, Quality and Regulatory Affairs Manager, Cochlear Ltd, Jun 17

Quality of speakers and ability to present very good.

Stefan Gaul, Head of Strategic Product Management, Haselmeier AG, Jun 17

A lot of focus on describing status of industry and issues but little insight into innovations and technical solutions. Some talks lacked technical depth with was disappointing.

James Gani, Design Team Leader, SPD Development Company Ltd, Jun 17

I feel the course was very useful and provided an good understanding of connectivity in medical technology and has opened my mind to the many challenges but benefit of connectivity in medical technology.

Paul Fitton, Regulatory Affairs Specialist, Presspart, Jun 17

Very well organised and a nice broad range of topics. Some very good speakers and interesting talks.

David Harris, Scientist and Inventor, PA Consulting, Jun 17

Provides wide overview, interesting presentations, well prepared speakers

Stefan Gaul, Head of Strategic Product Management, Haselmeier AG, Jun 16


Arnaud Guillet, Business Development Director , Biocorp, Jun 16

Very good

Arun Sarda, Global Director, QA & Regulatory Affairs, Presspart Manufacturing Ltd, Jun 16