Webinars

What Medical Device Manufacturers Can Learn From Past Vulnerability Disclosures

Topics:
Regulatory, Thought leadership, Vulnerability management
What Medical Device Manufacturers Can Learn From Past Vulnerability Disclosures
What Medical Device Manufacturers Can Learn From Past Vulnerability Disclosures
play icon
April 22, 2021
This is some text inside of a div block.
Time:

In December 2016, the FDA released a guidance document entitled Postmarket Management of Cybersecurity in Medical Devices, in which the FDA makes several recommendations to medical device vendors and healthcare delivery organizations on how to manage the cybersecurity risks introduced by connected medical devices. One of the recommendations is for device vendors to participate in cyber risk information sharing, in which information about security vulnerabilities is shared with the medical device community via Information Sharing Analysis Organizations (ISAOs). A medical device cybersecurity advisory issued by ICS-CERT can be the result of either self-reporting by the vendor or from a third party, like a researcher, via an ISAO or directly to ICS-CERT. For the past 3 years, MedCrypt has been analyzing this data and releasing it in an annual white paper. This webinar will dissect the findings and discuss trends and predictions for the future of medical device cybersecurity.

Speakers

Our team of FDA analysts and  cybersecurity experts provide robust and actionable cybersecurity roadmaps to ensure you meet FDA requirements. Get the Medcrypt advantage today!

Axel Wirth

Axel Wirth

CSS
Seth Carmody

Seth Carmody

VP of Regulatory Strategy
Vidya Murthy

Vidya Murthy

COO

More resources

Research, not marketing

We are dedicated to helping advance our industry’s understanding of the challenges and opportunities we face through research. Check out our whitepapers.

FDA, RTA and eSTAR - oh my!

Watch our latest webinar that discusses regulatory updates and the impact for medical device development and post-market management.