ModulesModule coverage

Quality management

Inspection plans, holds, non-conformance and corrective action, plus the certificates and traceability records a regulated customer or auditor will ask for. In food, pharma and aerospace this is not an optional module — it is what makes the system auditable.

35 of 53 profiled systems (66%)4 demo questionsReviewed September 2026

Add to a requirements draft

01Questions for the demonstration

Written to separate what is generally available from what is shown. Ask them in the order given; the later ones assume the earlier answers.

  1. Q1

    Can inspection be required at goods receipt, in process and before despatch, with the stock quarantined until it passes?

  2. Q2

    How does a non-conformance escalate into a corrective action, and can that be closed without evidence attached?

  3. Q3

    Can you trace a finished lot back to every input lot and forward to every customer shipped, and how long does that query take?

  4. Q4

    Are electronic signatures and audit trails to 21 CFR Part 11 supported in the core product or through an add-on?

02Systems offering it

35 of the 53 profiled systems document this module. Alphabetical; a listing is a documented fact, not an endorsement.