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Webinar · February 4, 2026

FDA ComplianceFDA Cybersecurity ReadinessSoftware Bill of Materials (SBOM)Vulnerability Management

Mastering Postmarket Surveillance: Why and How

Master the complexities of FDA & MDR postmarket requirements with expert-led insights.

Axel Wirth, Om Mahida

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About this webinar

What to expect.

Regulatory scrutiny is at an all-time high. Learn from industry veterans at BioT and Medcrypt as they demonstrate how to transform the "burden" of cybersecurity into a competitive advantage. Gain practical knowledge on managing firmware SBOMs, automating evidence collection, and streamlining remediation across the entire device lifecycle.

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Go deeper on the topics from this webinar with Medcrypt analysis and real device programs.

Know where you are in 1 hour.

Run the free check or talk to a human. Either way, you’ll get a clearer view of readiness without a paywall or lengthy sales call.

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