Based onv.20 Entreprise

A connected LIMS from order to report

Register, plan, collect, analyse, review and report every sample while governed automation coordinates routine work.

Evaluate with confidenceWe provide proofs of concept and demo instances so you can evaluate the LIMS against your laboratory’s workflows before committing to a full implementation.

Functional capabilities

What the platform does across laboratory operations.

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Sample & workflow management

Register samples, preserve custody, control states and know what must happen next.

Field sampling, logistics & emissions plans

Plan routes, field work, in-situ readings and controlled emissions-monitoring campaigns.

Laboratory analytics & QA/QC

Apply calculations, specifications, statistics, control charts and technical review.

Instruments & equipment

Connect supported equipment and govern calibration, maintenance and transfer exceptions.

QMS & controlled compliance

Manage nonconformities, CAPA, audits, documents, training and change control.

Documents & customer portal

Generate controlled, customer-specific reports and deliver authorised records securely.

AI & agentic operations

Let governed agents monitor queues, prepare work and escalate exceptions for human decisions.

Emissions analysis plan management

Manage approved emissions analysis plans from monitoring design through authorised report.

Supports controlled monitoring and evidence. Compliance depends on the applicable permit, jurisdiction, validated scope and laboratory procedures.

Sites, sources and monitoring points
Pollutants, methods, limits and frequencies
Recurring campaigns, calendars and routes
Field readings and operational metadata
Equipment and calibration readiness
Samples, filters, containers and custody
Laboratory analysis, calculations and QA/QC
Missed events, exceptions and rescheduling
Plan versions, approvals and audit history
Reporting schedules and portal delivery

Governed AI in the workflow

Agents can monitor deadlines, identify missing information, draft approved-data summaries and coordinate permitted actions. Authorised people retain every accountable decision.

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Industries

Where the platform is applied. Each industry uses the same functional foundation with project-specific methods, terminology and controls.

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Environmental monitoring

Water, wastewater, soil, air, emissions and noise.

Food, beverage & agriculture

Ingredients, products, crops, feed, soil and production quality.

Mining, metals & geosciences

Rocks, drill cores, ores, concentrates, metals and materials.

Molecular biology & biotechnology

Microbiology, genomics, biological samples and derived records.

Chemistry, petrochemicals & materials

Analytical chemistry, industrial QC, petrochemicals and material testing.

Gemology

Coloured stone intake, testing, grading, certification and verification.

Laboratory operating modelsResearch · Contract testing · Quality control · Multi-site service laboratories

Connect the laboratory around controlled data

Instrument and system compatibility is confirmed by model, software version, firmware and interface during project assessment.

Odoo-based technical structure

Customers, field users and laboratory teams
Lims.science samples, workflows, analytics, QMS, documents and AI
Applicable Odoo business modules
Supported Community or Enterprise deployment
Instruments, field systems, APIs and external platforms

Controlled workflows, qualified claims

Configurable controls can support ISO/IEC 17025, applicable OECD and EU GLP, EU GMP Annex 11 and data-governance requirements. Compliance remains scope- and validation-dependent.

Discuss the right project structure

Bring your workflows, methods, systems and priorities. We will map the right configuration and delivery approach.

Designed to support ISO/IEC 17025 and GLP-controlled work

A governed LIMS foundation for reliable results, attributable records and inspection-ready evidence.

ISO/IEC 17025

Methods, competence, equipment, metrological traceability, quality control and technical review.

GLP / BPL

Study plans, SOPs, raw data, deviations, QA evidence, reporting and archiving where GLP applies.

Scope & validation

The system supports readiness; accreditation and compliance remain the laboratory’s responsibility.

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