Building an Audit-Ready Secure SDLC

As medical devices become more complex—incorporating AI and increased connectivity—ensuring compliance with FDA and EU MDR requirements is more challenging than ever. Teams responsible for making sure products are safe and effective must manage intricate software supply chains, document SBOMs, and mitigate cybersecurity risks, all while maintaining end-to-end traceability. Without the right processes, compliance gaps can delay product releases and jeopardize patient safety. In this webinar, you will learn how to:

• Create end-to-end traceability across product security risks, requirements, and evidence of control verification
• Stay audit ready to meet FDA and EU MDR requirements and standards like ISO 27001
• Integrate your SBOM and vulnerability management tools into your SDLC for better traceability and risk mitigation

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