How to Get Started
Three ways to use ComplianceGxP — from a free community demo to a fully managed private instance on your own document library.
- Sandbox knowledge base with public regulatory content
- GAMP5, 21 CFR Part 11, EU Annex 11, ICH Q7/Q10
- QA mode — sourced answers with citations
- 10 free queries per day
- Demo API key on request
- Try before you commit
- Your SOPs, protocols & guidelines ingested
- Private namespace — isolated FAISS index
- All 4 modes: QA, Deviation, CAPA, CSV
- Full team access for 90 days
- GAMP5 validation package (IQ/OQ/PQ)
- 2 feedback sessions — shape the roadmap
- Everything in Private Pilot
- Ongoing maintenance & updates
- MCP & SHARP integrations
- Multi-tenant for CDMOs (per-sponsor isolation)
- SLA & dedicated support
- Change-control workflow built in
| Feature | Community | Private Pilot | Professional |
|---|---|---|---|
| Knowledge base | ✓ Public regulations | ✓ Your docs | ✓ Your docs |
| Private namespace / FAISS index | — | ✓ | ✓ |
| Source-cited answers | ✓ | ✓ | ✓ |
| QA mode | ✓ | ✓ | ✓ |
| Deviation, CAPA, CSV modes | — | ✓ | ✓ |
| GAMP5 IQ/OQ/PQ package | — | ✓ | ✓ |
| JSONL audit trail | ✓ | ✓ | ✓ |
| MCP & SHARP integrations | — | — | ✓ |
| SLA & ongoing support | — | — | ✓ |
| Cost | Free | Free | TBA · 2026 |
What the Pilot Covers
Pilot teams get full access to a private ComplianceGxP instance for 90 days — trained on their own document library, at no cost.
Document Ingestion
SOPs, validation protocols, regulatory guidelines, deviation records, training documents — your full compliance library indexed and searchable via AI.
4 Compliance Modes Active
QA for policy lookup, Deviation for structured 5M RCA, CAPA for corrective-action drafting, CSV for IQ/OQ/PQ protocol outlines.
GAMP5 Validation Package
IQ-CGXP-001 (16 test cases), OQ-CGXP-001 (33 test cases), and a PQ-CGXP-001 template scoped to your instance. Ready for inspection from day one.
Audit-Ready From Query One
Every query logged in JSONL with timestamp, user, mode, sources, and answer. 21 CFR Part 11 and EU Annex 11 traceability built in.
Qualifying teams: mid-size pharma, CDMO, or biotech in DACH/EU · GxP environment required · No contracts
Apply for Free PilotNot ready for a pilot yet?
Start with the free Community demo — no registration, no commitment. Try ComplianceGxP on real compliance questions right now.
Explore Community