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Navigating Cybersecurity during FDA eSTAR Submissions

Navigating Cybersecurity during FDA eSTAR Submissions

Navigating Cybersecurity during FDA eSTAR SubmissionsGarrett Schumacher, MS, CISSP
Published on: 06/08/2025

The FDA’s electronic submission system, eSTAR, requires structured cybersecurity artifacts for 510(k), de novo, and PMA submissions. Our guide shows how to complete each section, map your docs, and stay compliant with the latest expectations. Use these graphics and resources to navigate a critical process for getting your products to market.

CybersecurityBlogsSecurity Guides
Total Product Life-Cycle Security for Medical Devices

Total Product Life-Cycle Security for Medical Devices

Total Product Life-Cycle Security for Medical DevicesGarrett Schumacher, MS, CISSP
Published on: 04/08/2025

Cybersecurity isn’t just a test before launch. At Velentium Medical, it’s built into every phase of development and maintenance. Our Total Product Life-Cycle process ensures your device is secure by design and safe in the field, backed by our templates and expertise to help you navigate the full process.

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