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Microfilm produces signed, traceable QA evidence — captured as you test, mapped to every requirement. Below is how that same trail fits the regulated workflows teams come to us for. Each page links out to the guides that teach the standard itself.
Tamper-evident, attributable test records for software validation under FDA 21 CFR Part 11 — signed as the work happens, not reconstructed for the audit.
ExploreIndependent, attributable test evidence for IV&V teams — signed by the verifier who ran it, traceable to the requirement, separable from the development record.
ExploreAudit-evidence workflows for FedRAMP and CMMC environments — signed test records mapped to the control they support, exported as an assessor-ready package.
ExploreVerification records for medical-device software under IEC 62304 — each test traced to the requirement and software item it verifies, signed and audit-ready.
ExploreQA evidence for teams shipping with AI coding agents — a signed record of what was tested and why a change is trusted, and structured context agents can act on.
ExploreThese frameworks name the environments Microfilm is built for and the evidence it helps you produce — not certifications, authorizations, or attestations Microfilm itself holds. Software validation and any authorization decision remain your responsibility.
Walk through capture to audit-ready export, or download the free capture app and record your first session.