The operating system for regulated labs
The lab OS that replaces five tools,
passes your audit, and runs itself.
LIMS + ELN + QMS + Compliance + AI — built AI-native from day one, not retrofitted. Architecturally enforced 21 CFR Part 11. Per-tenant database isolation. Up in a day.
SQF · Pharma GMP · CLIA · ISO 17025 · 21 CFR Part 11
Proven in production at BRS Lab Services — Read the case study →
Most LIMS stop at features.
AILS enforces compliance architecturally.
The difference isn't the feature list. It's what happens when someone tries to bypass the rules.
Most LIMS let you issue a COA and then edit it.
Issued COAs are write-locked at the database layer. No edit, no re-issue — not even by platform admins. SHA-256 hash verifiable by your auditor.
Most QMS platforms use role-based access as their only gate.
Critical signatures require re-authentication at the moment of signing — not just a logged-in session. COA issue, SOP sign-off, COC acceptance all require password re-entry.
Most multi-tenant SaaS uses row-level filtering to separate tenant data.
Every lab gets a physically isolated database. Cross-tenant data access is architecturally impossible — not a policy you hope holds.
Most platforms bolt AI on as a chatbot after the fact.
AI embedded directly in regulated workflows — each agent scoped to your live lab data, each doing one specific job. Not a generic assistant. Not a chatbot.
Most LIMS vendors make you assemble a validation binder yourself.
The Vendor Validation Package is pre-built: RTM, 16 executed OQ test cases, IQ/OQ/PQ templates, and a §11.100(c) e-signature declaration letter — ready for your FDA submission.
Most platforms go dark at training expiry.
Expired training hard-blocks access to affected procedures. Not a warning. A hard block — enforced before the user can proceed.
Most LIMS have no EU data residency option and no GDPR compliance tooling.
EU data residency with signed Data Processing Agreement (EU Standard Contractual Clauses 2021). GDPR Article 5 data minimisation review — automated for EU-region tenants.
Enterprise security reviews mean sending emails and waiting weeks for a manual document.
ISO 27001-aligned security posture — downloadable PDF overview generated dynamically for enterprise due diligence. Always current, never stale.
We test everything we ship.
Every month. In public.
Most software companies tell you their platform is reliable. We run 341 automated end-to-end tests against our live platform every month and publish the results in the Platform Admin dashboard.
Test suites cover: Core QMS · COC/COA Pipeline · SQF / HACCP · Pharma GMP · CLIA · EMR Integration · Agricultural & Environmental · Construction Materials · ISO 17065 Cert Body · 2FA · Workflows · Analytics · Audit Trail · Security · and more.
Does your current LIMS have a score —
or just a sales rep?
Lab management is still broken in 2026.
Most labs run 5+ disconnected tools. COC in one system. COA in another. QMS in a binder. Compliance in a spreadsheet. AI nowhere.
Audit prep takes weeks
Assembling compliance records from 5 systems for a single inspection. Every time. Even when nothing changed.
Every tool is an island
COC, COA, QMS, equipment, and billing don't talk to each other. Manual reconciliation every day, on every result.
AI is bolted on everywhere else
Other platforms added a chatbot. We built 46 purpose-built agents into every workflow from day one — before the first user logged in.
The core workflows every accredited lab runs
COC · COA · QMS · Equipment · Invoicing · Client Portal — all connected. No manual reconciliation.
Core Lab Operations
The sample-to-result pipeline. COC creation, COA generation, client invoicing, client portal, and inventory — all connected.
- Chain of Custody (COC)
- Certificate of Analysis (COA)
- Client Portal & Invoicing
- Inventory Management
Quality Management
Full QMS stack — the equivalent of Q-Pulse or MasterControl, built into the same platform as your LIMS.
- CAPA & Deviations
- SOPs with AI Drafting
- Internal Audits & Proficiency
- Equipment, Training & Risk
AI That Does the Work
Each agent has one job. Each job used to take hours. 46 purpose-built agents scoped to your live lab data — not a generic chatbot.
- Regulatory Intelligence Engine
- Instrument CSV & Image Ingest
- IQ/OQ/PQ Validation Co-Pilot
- HACCP Plan Reviewer
Compliance & Validation
21 CFR Part 11 enforced at the architecture layer — not a configuration. SHA-256 COA hashing. Re-auth at signing. Append-only audit trail.
- 21 CFR Part 11 Enforcement
- Two-Factor Authentication
- Immutable Audit Trail
- Vendor Validation Package (IQ/OQ/PQ)
Platform & Integrations
Workflow automation, QuickBooks and Xero sync, SAP QM bridge, multi-site organization management, and analytics with AI-powered forecasting.
- Trigger-Based Workflow Automation
- QuickBooks & Xero Integration
- SAP QM — Bidirectional Integration
- Multi-Site Organizations
Industry Verticals
Add the regulated vertical your lab operates in. SQF, Pharma/GMP, CLIA, Cultivation, Agri-Env, Construction, and Certification Body are all live.
- Food Safety / SQF — Live
- Pharma / GMP — Live
- CLIA — Live
- Cultivation (GACP + FDA Ready) — Live
- Agricultural & Environmental — Live
- Construction Materials — Live
- Certification Body (ISO 17065) — Live
A complete QMS —
not an add-on.
CAPA, deviations, SOPs, internal audits, management reviews, and proficiency testing. The equivalent of Q-Pulse or MasterControl, built into the same platform as your LIMS.
See full QMS →AI that does the work. Not just the chat.
Each agent has one job. Each job used to take hours.
Regulation changes. Your SOPs update in 30 seconds.
Upload a new ISO 17025 revision. Claude maps every impacted SOP in your library by clause. What used to take a QA manager two days takes 30 seconds.
Validation binders that used to cost $50K. Now on click.
Describe your instrument. Claude writes the validation test steps, guides execution, and exports a complete IQ/OQ/PQ report — ready for your FDA submission.
HACCP audit prep: from 3 days to 30 minutes.
Claude scores your HACCP plan against SQF Code 9.0 and all 7 HACCP principles. Flags every gap. Writes your pre-audit action plan. In minutes.
Every COA reviewed before it leaves the building.
10-point AI compliance check against your accreditation standard — ISO 17025, CLIA, FSMA — on every COA, every time. Pass / Warning / Fail with exact clause references.
Your ISO §8.9 management meeting. Prepared in one click.
All 14 required agenda items auto-populated. AI pulls live data from CAPAs, equipment, deviations, and revenue. Talking points drafted. Minutes recorded. PDF exported.
Instrument data in the right COA the moment the run finishes.
Drop any instrument export. Claude maps columns to the right result fields and learns your format after the first import — no manual column mapping ever again.
Plus 40 more agents across OOS investigations, stability trends, batch release risk, CLIA QC, EMR integration, SQF self-audit, agri-env compliance, construction QC review, and more. See all 46 →
“We built AI Lab Services because we ran out of patience with legacy LIMS that cost $50,000 to implement and still required spreadsheets to manage day-to-day operations. Labs shouldn't have to choose between compliance and usability.”
Matt DeWolfe
Founder, AI Lab Services & BRS Lab Services
Add the vertical your lab operates in.
Everything else is already there. Verticals are module-gated add-ons — flip one switch and your platform gains a fully-built compliance layer for your regulated industry.
Food Safety
SQF Code 9.0 / HACCP
Full GFSI-recognized SQF compliance layer. HACCP plans, CCPs, PRPs, supplier SQF fields, and an AI self-audit that scores your facility against SQF clauses and writes your pre-audit action plan.
- HACCP Plans with AI Reviewer
- Critical Control Points & Monitoring
- Prerequisite Programs (PRPs)
- SQF Self-Audit + Action Planner
Pharma / GMP
FDA 21 CFR Part 211 / ICH
Full pharmaceutical-grade add-on. OOS investigations, ICH stability studies with OOT detection, method validation, batch release with AI risk scoring, change control, and a second-person COA review.
- OOS Investigations (Phase 1 & 2)
- ICH Stability Studies + Trend Interpreter
- Method Validation (ICH parameters)
- Batch Release with AI Risk Assessment
CLIA
42 CFR Part 493 — Clinical Laboratory
Full CLIA compliance layer. Patient result management, Westgard-rule QC, CAP/COLA proficiency testing with AI failure investigation, personnel qualifications, and a native HL7 FHIR R4 EMR integration agent.
- Patient Results + Critical Value Notifications
- QC Records + Westgard Rules + AI Trend Analysis
- Proficiency Testing + AI Failure Investigator
- EMR Integration — HL7 FHIR R4 (Epic · Cerner · Meditech)
Cultivation
GACP · FDA Schedule III Ready
Seed-to-harvest documentation for cannabis, hemp, and botanicals. Batch tracking, environmental logs, IPM records, dual-witness waste destruction, and a forward-looking FDA Schedule III readiness audit.
- Batch & Growth Stage Tracking
- Environmental & Nutrient Logs
- IPM + Approved Input Registry
- GACP & FDA Readiness Self-Audit
Agricultural & Environmental
EPA MCL · NELAP · OMRI
Soil, water, and environmental sample tracking with automatic exceedance detection against EPA MCLs and state action levels. A live AI Compliance Checker evaluates every result and flags violations with exact regulatory citations.
- Soil, Water & Environmental Sample Tracking
- Auto Exceedance Detection vs. EPA MCLs
- AI Compliance Checker — per-analyte findings
- Test Methods Expert — 20 EPA method templates
Construction Materials
ASTM · ACI 318 · AASHTO
Concrete, asphalt, aggregate, steel, and geotechnical testing with automated ASTM specification compliance review. An AI Construction QC Reviewer evaluates results against ASTM limits and returns structured accept / conditional-accept / reject recommendations.
- Concrete, Asphalt, Steel & Geotechnical Testing
- Auto Pass/Fail vs. ASTM Spec Limits
- AI Construction QC Reviewer — structured findings
- Field-to-report sample lifecycle tracking
Certification Body
ISO 17065 / IAF MLA / ILAC MRA
Full certification lifecycle management for product certification bodies. Application intake, impartiality risk screening, certificate issuance with public directory, and surveillance scheduling.
- Application Intake & Evaluation Workflow
- Impartiality Risk Screener (ISO 17065 §4.2)
- Immutable PDF certificate generation on issuance
- Public certificate verification directory — no login required
- Certificate Expiry & Surveillance Intelligence digest
- ISO 17065 complaint management
- Surveillance Scheduling & CAPA Linkage
Built inside a working lab. Not designed around one.
AI Lab Services wasn't designed by software engineers trying to understand lab workflows. It was built inside BRS Lab Services — dual-licensed accredited microbial testing facilities in Windsor, ON and Canton, MI — under real ISO 17025 and CLIA operational pressure. Every architectural decision reflects a constraint we lived with first.
Dual-Licensed Facilities
Accredited labs in Windsor, ON and Canton, MI — operating in both US FDA and Health Canada regulatory environments.
Operating in Both Jurisdictions
Per-tenant database isolation was designed before the first user logged in. Cross-border regulatory differences require it.
University Research
University of Windsor Beverage Lab — live institutional tenant since April 2026. Academic research and commercial testing on one platform.
Techcyte AI Partnership
AI-assisted microscopy analysis — 36+ species identified with machine precision.
Up and running in a day
No lengthy implementation projects. No consultants. No $50K setup fee.
Invite Your Team
Platform admin sends a tenant invite. The lab owner sets up their account, users, and branding in minutes.
Configure Your Lab
Add sample types, service types, test methods, clients, and disclaimers. White-label with your logo and colors.
Run Your Workflows
Create COCs, assign technicians, generate COAs, manage equipment, and bill clients — all in one place.
Transparent pricing from $79/month
No setup fees. No per-user gotchas. Cancel anytime.
See full pricing →Ready to see the infrastructure?
Six live environments. Pick your vertical. Real workflows, real data. No sales deck.