Change control

See what a change touches before anyone makes it.

Raise a change, assess its impact on validation, filings, training and documents, approve it and check it worked.

7-day free trial, no card required. Change control is in Professional and Enterprise.

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See it work

Follow one change

What is changing, and why

Describe the change and its driver.

Where it fits

Where change control fits

Changes often start from a CAPA or a deviation and end in new documents and training.

V5 AI

AI that sees it coming

It predicts and flags. Fixed rules decide. People sign.

AI in quality and the lab

See the next issue coming.

AI reviews deviation and complaint history to show where problems are building.

See V5 AI AI drafts and flags. A qualified person reviews and signs.
What's included

Everything in this feature

What change control uses, and which plan each item needs. Compare plans

  • Change register

    Professional and Enterprise

    Class, risk, status and effective date.

  • Impact assessment

    Professional and Enterprise

    Validation, regulatory, training, documents.

  • Approval and status history

    Professional and Enterprise

    Every advance kept.

  • Effectiveness check

    Professional and Enterprise

    Before closure.

V5 makes the impact visible. People decide whether the change goes ahead.

Sample report

Explore the sample records.

Open a sample report to review its contents, supporting references and how the record is built.

All sample reports and records
Free buyer guide12 pages · Online & printable · opens online

Quality Management Buyer Guide

For quality, regulatory and operations teams choosing quality management software. Use it with or without V5.

What's inside
  • Why quality systems stall
  • Issue-to-closure evidence map
  • Documents, revisions and training
  • Deviations, out-of-spec results and CAPA effectiveness

Plus Audits, complaints, supplier quality and traceability; Requirement vs configured workflow vs lab system; Risk-based evaluation, decision checklists, RFP and scoring.

We ask for your name and email so we can handle this request. The full guide then opens on this site, ready to translate, print or save. Privacy policy.

Guide page 6: out-of-spec result to investigation to CAPA, with effectiveness criteria examplesGuide page 4: eight-stage map from issue raised to human closure, with evidence and owner at each stageCover of the Quality Management Buyer Guide
Questions

Straight answers.

What buyers ask us first about Quality & Laboratory.

  1. Does V5 release product automatically?

    No. V5 gathers results and records for review, but a person in quality decides and signs the release.

  2. What does the lab side cover?

    Lab and QC covers sampling, instruments, methods, results and out-of-spec handling, with LIMS, lab notebook, stability and SPC on top. These are Enterprise features; see Compare details on the pricing page.

  3. Can we use V5 in a validated environment?

    For validation-controlled operations, V5's route is Enterprise private cloud with controlled upgrades and IQ/OQ support. Your team still validates V5 for its intended use.

Explore

More of the product

Start with one area. Add the rest when you are ready.

Try it with your next planned change.

Start a free trial or talk it through with us. No card needed.

Or (you can edit the question before sending).

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