Document control, approvals, training, audit management. Self-hosted or cloud. All modules included.
100%
audit-ready from day one
Low-code
build and scale your way
Since 2007
on the market
Industries
See how Comind.work fits your industry.
Quality management for pharmaceutical and biotech companies. From first QMS to enterprise compliance.
FDA 21 CFR Part 11, ICH Q10, GAMP 5, EU GMP Annex 11
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Quality management for medical device companies. Design controls, document control, and audit readiness for ISO 13485.
ISO 13485, EU MDR/IVDR, FDA 21 CFR 820, MDSAP
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Compliance and approval workflows for financial institutions. Audit-ready without enterprise GRC overhead.
SOX, Basel III, OSFI, PCI DSS
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Core capabilities
All included. No per-module upselling.
Version management, digital signatures, controlled document lifecycle.
Configurable approval chains, corrective actions, root cause analysis.
Training records, competency tracking, automatic assignment on document changes.
Change requests, impact assessment, approval routing, implementation tracking.
Internal and external audit workflows, finding tracking, evidence collection.
Compliance dashboards, regulatory reporting, trend analysis.
Built to grow
Start with the QMS you need now. When your operations outgrow standard modules, the platform extends.
When you need a process your QMS doesn't have a template for, build it. Same system, same audit trail.
Run on your own infrastructure. Full data sovereignty for GxP environments. Unique among QMS challengers.
Built on a process automation platform refined since 2007. Not a startup experiment - production-hardened infrastructure.
Complete compliance system - document control, approvals, training, audit management - configured in weeks.