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The digital twin for regulated laboratories

A LIMS that can prove it.

Every sample, instrument, method, analyst and procedure has a live electronic counterpart — and every change to any of them is signed, hashed and chained.

Built for laboratories that are inspected: pharmaceutical QC, environmental and drinking water, tissue banking, toxicology and contract testing. One core, twelve optional modules, and the validation evidence written alongside the code.

The physical laboratory and its digital twin, held in the DTL mark
At a glance
12
optional modules, licensed individually
15
regulatory frameworks mapped to mechanisms
5
pre-seeded workflow libraries to start from
28
report and certificate templates out of the box
21 CFR Part 11· EU GMP Annex 11· ISO/IEC 17025:2017· TNI / NELAP· ICH Q1A–Q1E· GAMP 5· ALCOA+
The platform
One system for operations, evidence and oversight

Analytical processes are authored as versioned, electronically signed workflow templates. A method change is a published template version, not a change request and a release cycle.

What the core carries →
Optional modules
Licence only the disciplines you practise

Twelve modules, each gated by its own activation key across both the interface and the API. Adding a discipline later is a key, not a project.

See all twelve →
Compliance
Every claim names its mechanism

Fifteen frameworks mapped to the mechanism that satisfies them — per-action signature policy, a verifiable SHA-256 hash chain, and audit findings that cite their clause.

The full regulatory scope →
Architecture
Cloud-native, and nothing to install

A stateless Node API over serverless PostgreSQL with row-level tenant scoping. Deploy multi-tenant, single-tenant in your region, or inside your own boundary.

How it is built →

See it against your own process

Forty-five minutes, screen-shared, with the person who built it. Bring a real SOP or method and we will model it live.

Book a demo