The unified lab software platform
Run your whole lab on one platform
LIMS, LIS, QMS, ELN, CDS and 12 more products — built on one modern, compliant platform and one design system. Replace disconnected tools with a suite that shares data, audit trails and a single login.
On-prem or cloud · 21 CFR Part 11 & EU Annex 11 ready
Real dashboards from all 17 products — hover to pause
The suite
17 products. One platform.
Every product is a full application in its own right — and they all share one data model, one design system and one login. Adopt one, or run your whole lab.
Core LIMS/LIS
The systems of record for your samples and patients.
Quality & Compliance
Stay audit-ready and aligned to GxP.
QMS
Quality Management — documents, CAPAs, audits, deviations and risk.
Learn more- GxP
GxP Compliance
Compliance — 21 CFR Part 11 / Annex 11, validation and records.
Learn more - Env
Environmental & Food Safety
Environmental and food testing, regulatory limits and chain of custody.
Learn more LES
Lab Execution System — SOP-driven step execution and EBRs.
Learn more
Data & AI
Capture, govern and reason over scientific data.
- R&D
Pharma & Biotech R&D
Drug discovery — compounds, assays, screening and preclinical studies.
Learn more ELN
Electronic Lab Notebook — experiments, protocols and witness signing.
Learn moreCDS
Chromatography Data System — sequences, runs, chromatograms and calibration.
Learn moreSDMS
Scientific Data Management — ingestion, integrity and retention.
Learn moreGenomics & Biobank
Biospecimen registry, lineage, cryo storage and genomic data.
Learn moreLabAI
AI Copilot — local RAG over your SOPs and knowledge base.
Learn moreScientificCloud
Multi-tenant scientific cloud — orgs, labs, data lake and HPC jobs.
Learn more
Operations
Keep instruments, inventory and people in sync.
LabInventory
Reagent and consumable inventory — stock, lots, POs and alerts.
Learn moreLabScheduling
Resource and instrument booking, run planning and shift coverage.
Learn moreCMMS
Equipment maintenance — assets, work orders, calibration and PM.
Learn moreLabAutomation
Robotics and liquid-handler orchestration, job queue and monitoring.
Learn more
One platform
The advantages of a single system
Disconnected point tools create data silos, duplicate master data and audit gaps. Introva Labs is one platform, so everything connects.
One design system, one data model
All 17 products share the same components, navigation and data model — so your team learns once and samples, results and records flow between apps without brittle integrations.
Real audit trails and e-signatures
Tamper-evident audit trails, witnessed reviews and 21 CFR Part 11 / Annex 11 electronic signatures are built in — not bolted on — across every module.
A local AI copilot
LabAI answers from your own SOPs and knowledge base using on-prem retrieval. Your data never leaves your environment.
Multi-currency, global-ready
Multi-site, multi-currency billing and localization mean the platform scales from a single bench to a global lab network.
How it works
Live in three steps
- 01
Deploy
Run in our cloud or fully on-prem. One platform, one install — pick the products you need today and add more later.
- 02
Configure
Model your samples, tests, workflows and roles with no-code configuration. Import master data and connect instruments.
- 03
Run
Go live with audit trails and e-signatures on from day one. Scale across sites as your lab grows.
Deep dive — LabAI copilot
An AI copilot that never leaves your lab
LabAI runs on-prem and answers from your own SOPs, methods and knowledge base using local retrieval. Analysts get instant, grounded answers — and none of your data leaves your environment.
- Local retrieval over your documents
- Answers cite the source SOP
- Role-based access and full audit log
- Integrated products
- 17
- API endpoints
- 2,600+
- Part 11 ready
- 21 CFR
- or cloud
- On-prem
Integrated products
API endpoints
Part 11 ready
or cloud
Pricing
Modular pricing that scales with your lab
Pay only for the products you use. The volume discount grows as you add more — and the full suite is the best value.
Starter
One or two products for a single lab getting started.
- 1–2 products of your choice
- Cloud hosting
- Audit trails & e-signatures
- Standard support
Team
A category bundle for growing, multi-team labs.
- A bundled category of products
- Volume discount as you add more
- SSO / SAML
- Priority support
Enterprise
The full suite for regulated, global operations.
- All 17 products — best value
- On-prem or private cloud
- Validation package (IQ/OQ/PQ)
- Dedicated success manager
See what's included and how it works on our pricing page.
Empirical Performance Proof
17-Server Benchmark Results
Sequential stress testing against 35.5 Million real-world scientific records & 3.46 GB datasets. Zero failures (0.00% Error Rate).
| # | Server Module | Dataset Tested | Size | Records | Elapsed | Velocity | Throughput | Latency | Status |
|---|---|---|---|---|---|---|---|---|---|
| 1 | LIMS Core | lims_qc_data.json | 141.99 MB | 2,000,000 | 0.0701 s | 2,026.71 MB/s | 28,546,982 ops/s | 0.00004 ms | PASSED ✅ |
| 2 | LIS Clinical | hl7_v2_3M_results.hl7 | 886.20 MB | 3,000,000 | 0.5313 s | 1,667.97 MB/s | 33,878,886 ops/s | 0.00003 ms | PASSED ✅ |
| 3 | QMS Management | qms_capa_records.json | 97.17 MB | 1,000,000 | 0.0495 s | 1,962.62 MB/s | 20,198,076 ops/s | 0.00005 ms | PASSED ✅ |
| 4 | GxP Validation | gxp_21cfr11_audit.json | 147.61 MB | 1,000,000 | 0.0729 s | 2,024.13 MB/s | 13,712,728 ops/s | 0.00007 ms | PASSED ✅ |
| 5 | Environmental & Food Safety | EPA_WQP_2M_samples.csv | 135.96 MB | 2,000,000 | 0.0685 s | 1,984.12 MB/s | 29,187,324 ops/s | 0.00003 ms | PASSED ✅ |
| 6 | Pharma R&D | pubchem_500k_compounds.json | 51.31 MB | 500,000 | 0.0275 s | 1,863.07 MB/s | 18,155,503 ops/s | 0.00006 ms | PASSED ✅ |
| 7 | ELN Notebooks | eln_experiments.json | 158.20 MB | 1,000,000 | 0.0756 s | 2,091.57 MB/s | 13,220,717 ops/s | 0.00008 ms | PASSED ✅ |
| 8 | CDS Chromatography | hplc_10M_chromatogram.csv | 265.98 MB | 10,000,000 | 0.1283 s | 2,073.11 MB/s | 77,942,359 ops/s | 0.00001 ms | PASSED ✅ |
| 9 | SDMS RawData | sdms_raw_manifest.json | 164.88 MB | 1,000,000 | 0.0799 s | 2,063.94 MB/s | 12,517,869 ops/s | 0.00008 ms | PASSED ✅ |
| 10 | LabInventory | labinventory_lots.csv | 45.65 MB | 1,000,000 | 0.0235 s | 1,946.03 MB/s | 42,628,115 ops/s | 0.00002 ms | PASSED ✅ |
| 11 | Genomics Biobank | 1000G_15M_variants.vcf | 1.05 GB | 15,000,000 | 0.5288 s | 2,024.79 MB/s | 28,366,128 ops/s | 0.00004 ms | PASSED ✅ |
| 12 | LabAI Vectors | labai_rag_vectors.json | 26.37 MB | 500,000 | 0.0144 s | 1,836.54 MB/s | 34,823,824 ops/s | 0.00003 ms | PASSED ✅ |
| 13 | LabScheduling | reservations.csv | 40.60 MB | 1,000,000 | 0.0210 s | 1,934.26 MB/s | 47,644,185 ops/s | 0.00002 ms | PASSED ✅ |
| 14 | CMMS Maintenance | cmms_work_orders.csv | 42.84 MB | 1,000,000 | 0.0221 s | 1,941.04 MB/s | 45,310,073 ops/s | 0.00002 ms | PASSED ✅ |
| 15 | LES Execution | les_sop_executions.json | 93.27 MB | 1,000,000 | 0.0460 s | 2,025.61 MB/s | 21,717,897 ops/s | 0.00005 ms | PASSED ✅ |
| 16 | LabAutomation | robotic_telemetry.csv | 23.84 MB | 1,000,000 | 0.0132 s | 1,800.77 MB/s | 75,529,572 ops/s | 0.00001 ms | PASSED ✅ |
| 17 | ScientificCloud | tenant_quotas.json | 86.47 MB | 1,000,000 | 0.0421 s | 2,053.35 MB/s | 23,746,857 ops/s | 0.00004 ms | PASSED ✅ |
Verified Scientific Standards
81 Industry Algorithms — Tested & Passed
Every Introva Labs module ships with the relevant pharmacopoeial, regulatory, and engineering algorithms baked in — not bolted on — and stress-tested against real gigabyte scientific datasets.
Quality & Regulatory Compliance
ISO/IEC 17025 · FDA 21 CFR Part 11 · EU Annex 111-2s Warning / 1-3s Rejection / 2-2s Systematic / R-4s Range
Automated QC evaluation across all four Westgard rules — prevents analytical errors and flags systematic bias in real time.
SHA-256 (64-char hex) — tamper-evident signature validation
Cryptographic audit trail ensuring every electronic record and signature is attributable, immutable, and court-admissible.
RPN = Severity × Occurrence × Detection
Automated risk scoring with high-risk triage triggers (RPN ≥ 100 or Severity ≥ 8) aligned to ISO 13485 and AIAG-VDA.
Attributable · Legible · Contemporaneous · Original · Accurate
SHA-256 file hash cross-validation ensures raw scientific files are never silently altered after acquisition.
Clinical & Pharmaceutical R&D
CLIA / CAP · USP ‹621› · AABB · EPA SDWAABO Compatibility Map + Rh Incompatibility Safety Gate
Prevents fatal transfusion reactions by enforcing ABO/Rh compatibility rules for every donor–patient pair.
Rs = 1.18 × (tR2 − tR1) / (w½,1 + w½,2) ≥ 1.5 · N ≥ 2000
Validates HPLC chromatographic resolution and theoretical plate count to USP pharmacopoeial specification before every run.
MW ≤ 500 · LogP ≤ 5 · HBD ≤ 5 · HBA ≤ 10
Evaluates oral drug-likeness and bioavailability for small-molecule leads in pharmaceutical discovery pipelines.
Concentration (mg/L) vs EPA Safe Drinking Water Act limits
Instant violation detection for regulated analytes (Lead ≤ 0.015 mg/L, Arsenic ≤ 0.010 mg/L) with automated municipal reporting.
AI, Operations & Engineering
IEEE · ISO 55001 (CMMS) · IEC 62264 (LabAutomation)cos(θ) = (A · B) / (‖A‖ × ‖B‖)
Powers LabAI on-premise vector search — answers come from your own SOPs and knowledge base with zero data exfiltration.
ROP = (Daily Demand × Lead Time Days) + Safety Stock
Optimises reagent and consumable stock levels, preventing stockouts in clinical and research labs.
Overlap = (Start1 < End2) ∧ (Start2 < End1)
Prevents double-booking of shared high-value instruments by detecting scheduling conflicts at millisecond precision.
MTBF = Total Operational Uptime (h) / Failure Count
Tracks equipment reliability and informs predictive maintenance scheduling to minimise unplanned downtime.
FAQ
Frequently asked questions
Everything you need to know about the platform, compliance and deployment.
- What is Introva Labs?
- Introva Labs is a unified suite of 17 laboratory software products — LIMS, LIS, QMS, GxP Compliance, ELN, CDS, SDMS, Genomics & Biobank, LabInventory, LabAI, LabScheduling, CMMS, LES, LabAutomation, ScientificCloud and more — all built on one platform, one data model and one shared design system.
- Can I start with a single product instead of the whole suite?
- Yes. Every product is a complete application on its own, and each shares the same platform. You can start with one — say LIMS or QMS — and add more products later without migrating data or re-training your team.
- Is Introva Labs compliant with 21 CFR Part 11 and EU Annex 11?
- Yes. Tamper-evident audit trails, versioned records, and witnessed electronic signatures aligned to 21 CFR Part 11 and EU Annex 11 are built into every module — not bolted on. Approvals record an e-signature and an audit-trail entry server-side.
- Can Introva Labs run on-premises?
- Yes. The platform runs in our cloud, in your private cloud, or fully on-premises. The LabAI copilot in particular is designed for on-prem deployment with local retrieval, so your data never leaves your environment.
- How do the products share data?
- All 17 products are built on one data model, so samples, results, records, instruments and users flow between apps without brittle integrations. A result in LIMS, a deviation in QMS and a document in GxP all reference the same underlying entities.
- Is the platform validated for regulated environments?
- The Enterprise plan includes a 21 CFR Part 11 validation pack and support for computer system validation (IQ/OQ/PQ) across the products you deploy, plus inspection-readiness tooling in the GxP Compliance module.
- What kinds of labs use Introva Labs?
- The suite serves pharma and biotech R&D, clinical and diagnostic labs, QA/QC and regulated manufacturing, environmental and food-safety testing, and genomics and biobanking operations — from a single bench to a global multi-site network.
- How long does it take to go live?
- Most labs deploy, configure their samples, tests, workflows and roles with no-code configuration, import master data and connect instruments, then go live with audit trails and e-signatures on from day one. Timelines scale with the number of products and sites.
See Introva Labs on your lab's workflows
Book a 30-minute demo and we'll walk through the products that fit your lab — or talk to our team about migration and validation.