Standard · ISO 9001:2015

ISO 9001, run as a three-stage workflow.

One workspace for the Quality Management System — from gap analysis against the clauses through evidence collection and the final assessment report. Roles split across creator, business liaison, GRC liaison and control owner. Editing follows the platform billing state.

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The three stages.

Stage 1 — Gap analysis
  1. Answer a clause-by-clause questionnaire across Clauses 4 to 10 of ISO 9001:2015.
  2. Capture an optional justification with each answer.
  3. Review the gap analysis — per-clause scores and the controls implicated by your answers.
  4. Submit. Stage 1 is the hard gate — the remaining stages unlock once it is submitted.
Stage 2 — Document readiness
  1. Open the catalog of every QMS document required — Quality Manual, procedures, work instructions, records.
  2. For each document, record its status — Available, Partial, Not Available, N/A.
  3. Optionally upload a controlled copy.
  4. Generate the Document Readiness Report.
Stage 3 — Evidence collection
  1. Capture evidence per control against the QMS clauses, assign owners, and upload files.
  2. Use AI-assisted policy drafting alongside to draft any missing policies.
  3. The GRC liaison fills the internal audit findings column — compliance status, notes, required actions.
Output — Assessment report
  1. At the end of Stage 3, generate a unified assessment report.
  2. The report rolls clause status, evidence references, audit findings and corrective actions into a single document.
  3. Export as .docx or .pptx.