V5 Ultimate
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Why V5? Product & Features
Why V5?Product & Features
  • Warehouse & TraceabilityReceive, store, pick and trace
  • Production & PlanningPlan jobs and guide production
  • Quality & LaboratoryTest, investigate and review
  • Documents & TrainingControl procedures and qualifications
  • Equipment & PerformanceMaintain assets and measure losses
  • Orders & IntegrationsConnect customers, suppliers and systems
  • Outputs & InsightsReports, KPIs and label design
Explore all industries
    • Bakery & Confectionery
    • Food Processing
    • Ingredients & Dry Mixes
    • Sausage & Meat Products
    • Produce Packing
    • Pet Food & Pet Supplements
    • Dairy & Chilled Foods
    • Beverages & Liquid Manufacturing
    • Infant Formula
    • Radiopharmaceuticals
    • Pharmaceutical
    • Medical Devices
    • Veterinary Pharmaceuticals
    • Blood & Tissue
    • Diagnostics & IVD Kits
    • Reference Materials & Standards
    • OTC Topical Creams & Gels
    • Dietary Supplements
    • Cosmetics & Personal Care
    • Cannabis & Hemp Manufacturing
    • Fragrances & Perfumery
    • Soaps & Personal Hygiene
    • Botanical Extracts & Essential Oils
    • Plastics & Resins
    • Agricultural Chemicals
    • Specialty & Industrial Chemicals
    • Printing Inks, Pigments & Construction Chemicals
    • Lubricants & Metalworking Fluids
    • Coatings, Adhesives & Sealants
    • Consumer Products
    • Electronics & Electrical Assembly
    • Textiles & Nonwoven
    • Contract Manufacturing & Co-Packing
    • Packaging & Food-Contact Materials
    • Regulated Warehousing & Distribution
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Audit Management · Internal · Supplier · Third-party

Audit management software with every finding routed straight to CAPA.

Plan the audit schedule for the year. Run internal, supplier, and third-party audits from one inbox. Evidence is hash-chained. The inspector logs in, sees what they need, and leaves.

Start a free trial See the audit module
  1. Annual Audit Plan

  2. Execute audits in-app

  3. Supplier Audits

  4. Auditor + Auditee Roles

Audit lifecycle, end to end.
Full product detailCommon problems, what's included, why teams choose it, and where commercial meets regulated.+
If any of these sound familiar

You're shopping for audit management software because audit week shouldn't be a fire drill.

Audit schedule lives in someone's Outlook calendar

Audit reports get emailed around and lose their attachments

Third-party audits arrive with no traceable evidence trail

Last inspection cited inadequate internal audit coverage

What's in the box

Audit lifecycle, end to end.

Annual Audit Plan

Risk-based schedule across sites, processes, and suppliers. Coverage gaps are visible, not invisible.

Execute audits in-app

Checklist by audit type (ISO 13485, GMP, BRCGS, SQF, internal). Evidence attached at the finding, not after the fact.

Supplier Audits

Schedule, execute on-site or remotely, attach evidence, score, and feed into supplier qualification status.

Auditor + Auditee Roles

Role-based visibility. Auditors see everything, auditees see their finding, executives see the dashboard.

Hash-Chained Audit Trail

Inspectors can verify nothing was edited after the fact. Required for Part 11, ISO 13485, and BRCGS.

What changes the day this goes live

Audit management changes how audit week feels.

  • Supplier audits actually happen — on schedule, with evidence
  • External auditor leaves the same day they arrived
Regulatory anchor

Aligned with every audit framework you'll face.

ISO 9001:2015

Document control (7.5), competence (7.2), nonconformity & CAPA (10.2), internal audit (9.2), management review (9.3) — all modeled, all evidenced.

ISO 13485:2016

Design controls, DHF/DHR/DMR, risk management hooks (14971), CAPA, post-market — same engine, device-grade controls.

BRCGS / SQF / FSSC 22000

Food-safety audit frameworks modeled — clause-mapped checklists, finding categories, and required evidence.

Questions buyers actually ask

Audit management software, answered.

What is audit management software?+

Audit management software is the system of record for planning, scheduling, executing, and closing internal, supplier, and third-party audits. It connects findings to CAPAs, tracks coverage, and gives inspectors a verifiable evidence trail.

Does V5 cover ISO 13485 and GMP audits?+

Yes — clause-mapped checklists for ISO 9001, ISO 13485, 21 CFR Part 820, Part 211, EU GMP, BRCGS, SQF, and FSSC 22000.

Can we run supplier audits in V5?+

Yes. On-site, remote, or hybrid. Evidence attaches at the finding, scores feed supplier qualification, and CAPAs route to the supplier portal.

How does audit management integrate with CAPA?+

Every audit finding opens a CAPA on close — same record, same effectiveness check, same closure lineage. No re-keying, no Excel.

Do auditors need a V5 license?+

External auditors get a free read-only license for the duration of the audit. They see exactly what's in scope, nothing else.

Capabilities vary by plan and setup. Confirm specifics with our team before relying on them.

Make the next audit boring.

Free trial. Real audit module.

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Next Step

Try V5 with your own records, or ask a question first. Ask V5 opens with an editable question; nothing is sent until you choose to.

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V5 Ultimate
Ultimate

Warehouse, quality and manufacturing software for regulated operations.

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Page version 1.2· Last revised 28 Sep 2026