Secure Product Development Framework
End-to-end secure development lifecycle the FDA expects to see referenced and evidenced in every cyber device submission.
DAST tooling combined with manual penetration testing - broader coverage with verified findings and minimal false positives.
250+ FDA submissions. Zero rejections.
Every dynamic application security testing (dast) engagement ships with the artifacts FDA reviewers expect to see - traceable, complete, and aligned with current guidance.
Every dynamic application security testing (dast) engagement produces evidence aligned to the regulatory and consensus standards FDA reviewers and notified bodies expect to see - traceable, complete, and ready to drop into your ISO 13485 quality system.
End-to-end secure development lifecycle the FDA expects to see referenced and evidenced in every cyber device submission.
Verification requirements for web and application security controls.
Defines the SPDF, Section 524B submission package, threat modeling, SBOM, security architecture views, and cybersecurity testing every cyber device submission must include.
Reference methodology for planning, executing, and reporting security testing.
End-to-end FDA premarket cybersecurity package for Software as a Medical Device - cloud, mobile, and web SaMD.
View SaMD CybersecurityThick client, thin client, mobile, and web app coverage.
View Application Penetration TestingFront-end, back-end, API, and mobile coverage in one engagement.
View Web Application Penetration TestingDAST tooling combined with manual penetration testing - broader coverage with verified findings and minimal false positives.