Quality & Compliance
QMS
Deviations, CAPA, audits — scored live, signed under Part 11.
Inspection plans and control points, NCRs and CAPAs, deviations and change control, complaints and audits, training and exams, environmental monitoring and stability, batch release and DSCSA — with a readiness scorecard that probes your real records.
What's inside
19 capabilities in QMS — every one a real surface in the product, not a roadmap item.
- Inspection Plans
- Control Points
- Inspections
- NCRs
- CAPAs
- Batch Release
- DSCSA Serialization
- Documents
- Risk Assessment
- Supplier Quality
- Complaints
- Audits
- Training
- Training Exams
- Environmental Monitoring
- Stability Studies
- Audit Trail Review
- Mock Recall
- Settings
See it in action
Not a dashboard tour — the actual working screens in QMS, on live demo data.
Who it's for
Quality teams under FDA / ISO who need workflows, not a binder.
See QMS on your own data.
Book a demo