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