Considering a new SBOM vulnerability management tool? Here's what to look for!
New case study

Considering a new SBOM vulnerability management tool? Here's what to look for! New case study

New case study

For Medical Device Manufacturer (MDM) product security experts tasked with ensuring the safety and security of products in the field, selecting effective tools is essential. While there are numerous options available, this case study explores how Medcrypt’s SBOM and Vulnerability Management Tool, Helm, offers enhanced accuracy in vulnerability detection compared to an open-source alternative. Spoiler alert:?In comparison to alternative tools,?Helm demonstrates superior performance?by delivering a larger number of valid vulnerabilities relevant to the medical device outlined in the SBOM. See the details in this new case study.

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New blog

It's not easy to know what to look for in an SBOM and vulnerability management tool. Choosing the right tools can make all the difference in identifying and mitigating risks effectively. Read the medical device manufacturer buyers guide to learn what to look for:

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Upcoming webinar

Navigating Medical Device Cybersecurity Waters: Regulatory Similarities and Differences Between the EU and US Although global medical device regulators have increasingly provided regulations and guidance on cybersecurity there are notable differences in the way regulators include cybersecurity, and related safety concerns, in their overall regulatory framework. Yet, similarities exist that allow medical device manufacturers to optimize their cybersecurity efforts and address multiple global regulations at the same time. The speakers from Medcrypt and the Johner Institut are recognized experts in their respective regions with a deep background in medical device regulations and cybersecurity. What you'll learn:

  • Different regulatory approaches EU vs US
  • Cybersecurity key components: MDR / IVDR (MDCG) vs. FDA
  • Similarities and differences in regulations
  • Unique aspects of FDA / MDR through examples
  • What this means for Medical Device Manufacturers that plan to launch products in EU, US, or both

The session will end with a live Q&A. Register for free to join us on May 2 at 16:00 CET / 10 AM ET / 7 AM PT. Email [email protected] for any questions.

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