Stay ahead of supplier risk
Spot recurring issues early and focus your attention on the suppliers that need it most.
Supplier Audit and Risk Management Platform
One place for every audit
Audits by our GxP auditors, managed in one platform, from audit request to supplier risk decision.
Why Audit Docs
One platform. A clearer view of every supplier.
Audit Docs gives your quality team one view of every supplier: its audit reports, findings, open CAPAs, and risk rating. Decisions take less time, and each one is backed by audit evidence.
Accelerate supplier qualification
Reports, findings, and CAPA status are ready when you need them, so qualification keeps moving.
Make better use of your audit budget
Spend your audit budget on the sites that have no coverage yet.
Experienced GxP auditors
Our auditors cover GMP, GDP, GLP, GCP, and gap assessments, and hold credentials such as CQI‑IRCA, ECA, ASQ, and ISO lead auditor qualifications.
Quality leadership behind every audit
Every audit report is reviewed by experienced quality professionals.
One team from report to closure
One audit team manages your audit from request to closure, so nothing gets lost along the way.
Audit Management
Audit faster. Qualify suppliers sooner.
Everything from audit request to CAPA closure happens in one place, with our quality team at every step.
Buy the report and assess the supplier now, instead of waiting for a new audit.
Where no report covers the site, request an audit and our quality team plans and carries it out.
Each CAPA response is reviewed and tracked until the observation is closed.
AI‑Powered Supplier Risk Intelligence
See supplier risk earlier. Decide with evidence.
AI organizes audit findings and risks into a clear view of each supplier.
Supplier risk profileLast audit · Mar 2026
Ostrevia Therapeutics
OverallMEDIUM
- Quality management systemLow
- Data integrityHigh
- QC laboratoryHigh
- Production and process controlMedium
- Warehouse and materialsLow
- DocumentationMedium
Rated by the lead auditor. Anonymized example.
CAPAs3 open · 1 closed
- CAPA-01 · Data integrityDisable shared logins on HPLC workstationsOVERDUE
- CAPA-02 · QC laboratoryDefine audit trail review frequencyIN REVIEW
- CAPA-03 · ProductionRevalidate drying step after equipment changeOPEN
- CAPA-04 · DocumentationUpdate batch record templateCLOSED
Each CAPA is linked to the audit observation it addresses
Supplier risk profiles
Quality areas rated by the lead auditor, with an overall rating for each supplier site.
Recurring patterns
See deviations that repeat across a supplier's audits and, where data allows, across its other sites.
Prioritize where it matters
Rank suppliers by risk, so new audits go to the sites that need them most.
Stay ahead of renewals
See report expiry dates and open CAPAs ahead of time, so you can plan requalification before reports expire.
AI helps surface the signals. Your quality team makes the decision.
Customer Testimonials
What better audit visibility means for quality teams.
Hear from the people using Audit Docs to manage supplier audits, strengthen qualification processes, and make better quality decisions.
“Before we commission an audit now, we check the library first. When a report already covers the site, we buy it and our assessment starts that week.”
“Every audit, its findings, and the CAPAs still open sit in one view. Qualification reviews take less chasing and more deciding.”
“Findings arrive structured and traceable to the report, so quality leadership can see where attention is needed across the supplier base.”
See how Audit Docs fits your supplier qualification process.
Bring your supplier list. We'll show you how Audit Docs supports your qualification process, from finding a report to CAPA closure.