Documentation

From new account to your first released result — configure by chat, register a sample, enter results, issue a COA.

A printable, phase-by-phase checklist: governance, roles, test catalog, QC criteria, data migration, validation, go-live.

Put a single-file uploader on any instrument PC and export files flow into Aliquora automatically — pairing keys, scheduling, troubleshooting.

How Aliquora's AI works: strict tenant isolation, opt-in data access, retrieval with citations, and human-approved actions.

Authenticate with API keys and automate samples, results, instrument uploads, and reference data over the REST API.

Subscribe an HTTPS endpoint to lab lifecycle events — payloads, HMAC signatures, idempotency, retries.

Requirement-by-requirement mapping of Aliquora's controls to FDA 21 CFR Part 11 and ALCOA+.

Clause-by-clause mapping to the management and technical requirements of ISO/IEC 17025:2017.

Customer-executed Installation, Operational, and Performance Qualification protocol templates.

A concise packet summarizing Aliquora's security and data-integrity controls for your review.

What Aliquora provides vs. what your lab must validate, document, and own.

Client, material type, project, collection details, and the tests to schedule per sample.

Material type names and descriptions for your sample catalog.

Test definitions with codes, units, methods, spec limits, and turnaround days.

Bulk result entry keyed by sample tracking ID and test code.