QualifyDoc collects, reads, and tracks supplier compliance documents so your quality team can stop living in email and start being audit-ready by default.
No new processes. No retraining. Your team gets the time back.
Start a conversationSuppliers send CoAs, audit reports, and certificates to a dedicated intake address. No portal training. No behavior change. Documents flow in the way they already do.
Key fields like lot numbers, expiry dates, and test results are extracted and checked against your requirements. Discrepancies are flagged before they become findings.
Automated tracking and chase notifications ensure certificates are renewed before they lapse. No more calendar reminders. No more scrambling.
Every document, every version, every action, logged with a complete audit trail. When FDA walks in, your supplier records are already waiting.
"QualifyDoc is a decision-support tool, not a decision-making tool. Your quality team stays in control. The software does the work they shouldn't have to."
QualifyDoc is built for mid-market pharma companies, CDMOs, and biotech companies managing 50+ active suppliers. Teams that are ready to move past Excel and email without taking on a 12-month enterprise implementation.
If your quality analysts are spending time chasing PDFs instead of doing quality work, we should talk.