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.
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.