Managing Cybersecurity Across the MedTech Lifecycle

As medical devices become increasingly connected and software-driven, cybersecurity cannot be treated as a final compliance checkpoint. It must be integrated throughout the entire product lifecycle, from requirements and design to development, regulatory submission, and post-market support.

Join experts from PTC and MedCrypt to explore how MedTech manufacturers can embed cybersecurity into product development processes while improving collaboration across engineering, quality, regulatory, and security teams. Attendees will learn how end-to-end traceability and a lifecycle approach can help organizations address evolving FDA and European cybersecurity expectations, reduce risk, and deliver secure, compliant medical devices more efficiently.

Broadcast: September 23rd, 2026: 11:00 AM – 12:00 PM EDT

Hosted by:

Sponsored by:

Who Should Attend: 

  • Medical device and diagnostic manufacturers, connected-device and software-enabled product companies, digital health and SaMD organizations, and MedTech contract design or manufacturing partners responsible for product cybersecurity and regulatory compliance
  • Chief Information Security Officer, Chief Technology Officer, and Chief Product Officer
  • VP/Director of Product Security or Medical Device Cybersecurity
  • VP/Director of R&D, Engineering, Product Development, Systems Engineering, or Software Engineering
  • Cybersecurity Engineers, Product Security Engineers, and Security Architects
  • Systems, Requirements, Software, and Test/Verification Leaders
  • Post-Market Surveillance, Vulnerability Management, and Product Support Leaders
  • Digital Transformation, PLM, and Lifecycle Management Leaders

Learning Objectives: 

  • Integrate cybersecurity throughout the medical device lifecycle, from requirements and design through post-market support.
  • Improve collaboration and accountability across engineering, quality, regulatory, and security teams.
  • Establish end-to-end traceability between cybersecurity requirements, risks, design controls, testing, and evidence.
  • Address evolving FDA and European cybersecurity expectations more efficiently.
  • Reduce cybersecurity risk while supporting the delivery of secure, compliant medical devices.

Speakers:

René Zöelfl
Global MedTech Industry Advisor | PTC

Axel Wirth
Chief Security Strategist | MedCrypt

Secure your spot for this webinar. The webinar will be recorded and all registrants will receive a link to the recording. Attendees to the live broadcast will be able to ask questions and receive a certificate of attendance.