Every module you need for
audit readiness
Complete QMS with all modules included. No per-module upselling. Configured for your processes in 21 days.
Complete QMS with all modules included. No per-module upselling. Configured for your processes in 21 days.
A complete compliance and quality management system built for regulated companies that need audit-ready systems.
Document control, CAPA, training, change control, audit, complaints
Electronic signatures, audit trails, access controls
Not a sandbox - a working QMS recording quality activities
Add custom workflows and integrations as your needs evolve
Each module addresses a specific quality management requirement for regulatory compliance.
Version management, digital signatures, SOP lifecycle. 21 CFR Part 11 compliant audit trails for every document.
Corrective and preventive actions with root cause analysis, effectiveness checks, and regulatory reporting.
Training records, competency tracking, automatic assignment when documents change. Always audit-ready.
Change requests with impact assessment, approval routing, and implementation tracking across your quality system.
Internal and external audit workflows, finding tracking, evidence collection. Ready for ISO 13485 and FDA inspections.
Complaint intake, investigation workflows, regulatory reporting. MDR and MedWatch compliant.
Complete QMS - document control, CAPA, training, change control, audit management - configured in 21 days.