Testing labs
You run the lab. One platform handles sample intake, results, certificates of analysis and your quality system, with a tamper-evident audit trail.
Starting at $299/month.

What you get
- Certificate of Analysis — Certificate of Analysis authoring, review and SHA-256-locked issuance.
- Chain of Custody — Chain of Custody: sample intake and ASTM D4840 custody transfer with signed handoffs.
- Equipment & Calibration — Equipment register with calibration and maintenance tracking.
- CAPA Workflow — Corrective and Preventive Action workflow (ISO 9001:2026 cl. 10.2).
- SOP Library — SOP library with versioning, review and sign-off, enforced at COA issue and other signing actions.
- System Test Suite — Platform system-test suite (1,232 tests across 102 suites as of the latest run).
- Immutable Audit Log — Write-once audit log at the application layer — tamper-evident today, not yet cryptographically immutable end to end.
Proof for your world

Everything for testing labs — 103 features
- Bench Sheets (Dictation)
- Certificate of Analysis
- Chain of Custody
- Client Management
- Client Portal
- Custom Fields Engine
- Departments & Cost Allocation
- Document Translation
- Electronic Lab Notebook
- Engagement Documents
- Equipment & Calibration
- Field Data Capture
- Image/Photo Evidence
- In-App Chat
- Inventory Management
- Invoicing & Accounting Sync
- Job Workspace
- Measurement Uncertainty (GUM)
- Method Validation Studies
- Product Library
- Quotes, Tenders & Contracts
- Report Builder
- Report Disclaimers Engine
- Report Generation & Delivery
- Report Template Engine
- Reserve Sample Tracking
- Sample Type Catalog
- Service Type Catalog
- Test Journal (ELN Entries)
- Test Method Library
- Test Report Authoring
- CAPA Workflow
- Change Control Workflow
- Complaint Handling
- Deviation Management
- ISO 9001:2026 Readiness
- Internal Audit Program
- Management Review Meetings
- Performance Benchmarks
- Proficiency Testing
- QMS Foundation
- Quality Culture
- Risk Assessment Register
- SOP Library
- Supplier Qualification
- Supplier Scorecards
- System Test Suite
- Tenant Self-Service Test Runs
- Training Records
- Validation Executions
- Validation Package
- Agricultural & Environmental Testing
- CCP Monitoring Logs
- CLIA Compliance
- CLIA EMR/EHR Integration
- Construction Materials Testing
- Critical Control Points
- Cultivation Compliance
- FAIR Data Export
- HACCP Plans
- ICH Stability Studies
- ISO 14001 Environmental Management
- ISO 45001 Occupational Health & Safety
- Institution Administration
- Institutional Lab Mode
- Out-of-Specification Investigations
- Pharma Batch Release
- Pharma GMP Module
- Prerequisite Programs
- Regulatory Update Feed
- SQF Food Safety
- Standards Library
- Standards Registry
- IEC Electrical Testing
- Accounting Integrations
- CSV Mapping
- Connections Hub
- Global CSV Mapping
- Ingest API
- Workflow Automation
- EU AI Act Article 50 Disclosures
- EU AI Act Assessment
- Fundamental Rights Impact Assessment
- ISO/IEC 42001 AI Governance
- API Key Management
- Agreements (BAA/DPA)
- Authentication & 2FA
- Immutable Audit Log
- Multi-Org Administration
- Post-Quantum Readiness
- Single Sign-On
- Tenant Lifecycle & Self-Healing
- Trust Loop
- Analytics & AI Insights
- Audit Readiness
- Dashboard Alerts
- Decision Engine
- My Work Inbox
- Platform Announcements
- Readiness Score
- Scheduling Intelligence
- Support Tickets
- Grants Management
Pages for your sector
Food Safety (SQF)
SQF-aligned chain of custody, COA issuance and HACCP-ready quality records.
Pharmaceutical / GMP
21 CFR 211 and ICH-aligned batch records, OOS investigations and stability tracking.
Clinical Laboratory (CLIA)
42 CFR Part 493 personnel, QC trending and proficiency testing for clinical labs.
Agricultural & Environmental
Soil, water and environmental sample testing against EPA and state frameworks.
IEC Electrical Testing
IEC-formatted electrical test reports and CB Scheme certificate issuance.
Water & Wastewater
Drinking water and effluent compliance with automatic MCL exceedance detection.
Academic & Research
Grant cost allocation, FAIR data publishing and academic terminology on the same core LIMS.
Frequently asked questions
How long does implementation take?
Most labs are fully operational within 1–2 business days. We handle the initial configuration, and your team can start entering COCs and generating COAs the same day your account is activated. There is no lengthy onboarding project or professional services engagement required.
Can I migrate data from my existing LIMS?
Yes. We support CSV import for clients, samples, and historical COC/COA records. For larger migrations from systems like LabWare, STARLIMS, or custom spreadsheet workflows, we can assist with a structured data import. Contact us to discuss your specific situation.
What is your audit trail coverage?
Every significant action in the platform is logged to a tamper-evident, hash-chained audit trail: record creation, edits, status changes, user logins, permission changes, and data exports. Logs include timestamp, user identity, action type, affected resource, and before/after values where applicable. Audit logs are accessible to admin users and can be exported for external review.
How do we prove 21 CFR Part 11 compliance for an FDA inspection?
AI Lab Services gives you two tools. First, the 21 CFR Readiness Assessment — an AI-powered audit that analyzes your live system data (audit logs, electronic signatures, SOPs, training records, CAPAs, and more) across 10 21 CFR Part 11 categories and returns a scored report with specific findings and recommendations. You can run it anytime and download a printable report. Second, the Vendor Validation Package (VVP) — a pre-built IQ/OQ/PQ documentation bundle that includes a Requirements Traceability Matrix, OQ protocols your quality function executes and signs, PQ templates, and the electronic-signature controls and documentation supporting your own §11.100(c) certification — ready to complete and include in your Computer System Validation binder for FDA submissions or internal audits. AILS supplies the vendor documentation; the validation itself is performed by you. Both are available on the 21 CFR module.
