Medical device cybersecurity

Security that moves with your product.

Practical product security support for medical device teams, from architecture and evidence reviews to ongoing vulnerability management.

Who this is for

A specialist alongside your team.

Engineering, product security, quality, and regulatory teams approaching a release, submission, or program transition.

What the work can produce

A product-specific evidence inventory and prioritized action plan

Threat models and security requirements connected to your architecture

A defined SBOM and vulnerability-handling workflow

Clear responsibilities for verification and ongoing security

A practical beginning

Start with a defined scope.

Start with a readiness sprint for one product and one milestone. Review the architecture, existing security work, and evidence with the people who own them. Then agree on the next implementation workstream.

Specialist testing, complete submission preparation, and remediation are scoped separately. Regulatory decisions remain with your responsible team. An engagement does not guarantee regulatory acceptance.

A useful next step

Connect the ideas to your work.

Start with your product, your team, and the milestone ahead.