The whole quality loop, one coherent system.
Qability combines document control, training, corrective actions, and audit-ready evidence into a single platform designed for regulated organizations.
Every SOP, controlled and current.
Manage SOPs, policies, and quality records with version history, electronic approvals, and centralized access. Effective and superseded states are always unambiguous.
- Version history & change control
- E-signature approvals
- Periodic review reminders
Close the loop on every finding.
Capture nonconformances, drive root-cause analysis, and track corrective and preventive actions through a repeatable, verifiable workflow with full visibility.
- Structured RCA templates
- Effectiveness verification
- Linked evidence & due dates
Competency you can prove.
Assign training the moment a document changes, track completion in real time, and keep evidence tied to people, roles, and certification requirements.
- Auto-assign on document change
- Live completion tracking
- Role-based curricula
A record auditors trust.
Every change, approval, and activity is captured automatically in a tamper-evident trail — so auditors see a complete, trustworthy history of your quality controls.
- Tamper-evident logging
- Who, what, when, why
- Export-ready evidence
And more
Built for the entire quality program
Beyond the core, Qability covers the workflows regulated teams rely on every day.
Risk & RCA
Risk registers, FMEA, and structured root-cause analysis built in.
Supplier quality
Approved supplier lists, scorecards, and supplier CAPAs in one place.
Inspections
Configurable checklists with pass/fail logic and evidence capture.
Workflows
Map your exact approval routes with conditional, role-based steps.
Real-time sync
Consistency across teams, sites, and departments — instantly.
AI sidecar
Draft SOPs, summarize CAPAs, and answer audit questions in seconds.
Designed for clarity