FDA 21 CFR Part 11 · EU Annex 11 · ISO 13485

Compliance implementation, simplified

ComplyFlow gives life sciences, medtech, and pharma teams one controlled workspace for validated implementation projects, QMS documents, tasks, and traceability.

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Validated ERP rollout

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Built for conservative regulated teams

Every implementation artifact in one controlled flow.

Validated templates

Start from IQ, OQ, PQ, validation plans, SOPs, risk assessments, and trace matrices with QMS-ready structure.

Project tracking

Track implementation tasks, evidence gaps, completion percentage, owners, and milestones across validated systems.

Audit-ready docs

Keep every project document tied to templates, versions, statuses, and traceability evidence for inspection readiness.

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Template libraryIQ, OQ, PQAll validation + QMS templates
Change controlNot includedVersion history + impact workflow
ApprovalsBasic status trackingApproval workflow + comments
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