Webinar: Medical Devices Security - Regulations and Practical Approaches
Watch this webinar back to get more clarity on these topics and find
out more about the state of the art concerning cybersecurity in medical devices, while also learning more about the current state of regulations &
practical approaches regarding the security of medical devices.
About the webinar
This webinar highlighted the need to implement cybersecurity
controls in medical devices. This comes both from the perspective of
minimizing the high risks associated with these types of products, as
well as meeting the mandatory regulatory requirements in place. The
webinar treated in more detail the regulatory environments for
medical devices in the EU (governed by the EU MDR) and USA (governed by
the FDA). Furthermore, the most relevant standards for approaching
cybersecurity in medical devices, including IEC 62443 and UL 2900 were
discussed in this interactive session, followed by some poll questions
along the way.
- Overview of medical devices cybersecurity risks
- Medical devices security regulatory requirements
- Most relevant standards to address medical devices security
- Recommendations for medical devices developers
- Conclusion and Q&A
For questions, please contact email@example.com. Curious to see what other webinars we have planned in the past? Visit: https://www.secura.com/webinar...