Ordo
Ordo Labs provides a data automation platform for regulated laboratories that connects directly to instruments, LIMS, and spreadsheets to auto-fill study reports with full traceability. Every value in a generated report links back to its original source file, and an immutable audit trail supports GLP, GMP, and ISO/IEC 17025 compliance. The platform includes a natural-language data agent that builds and executes data-processing steps from plain-word instructions.
- Software Only
- AI Agents
- Artificial Intelligence
- Regulatory & Compliance Technology
Funding
Founders
Founder details are not available yet.
Product
Problem
Regulated laboratories operating under GLP, GMP, and ISO/IEC 17025 standards spend excessive time manually transcribing data from instruments, LIMS, and spreadsheets into study reports. This process is error-prone, creates traceability gaps, and delays final sign-off, especially in high-throughput environments like bioanalytical CROs and manufacturing quality teams.
Solution
Ordo Labs provides a data automation platform that connects directly to laboratory instruments, LIMS, and spreadsheet files to auto-fill study reports as runs are conducted. Every value in the generated report is linked back to its original source file, eliminating retyping and ensuring full traceability. The platform supports plain-language instructions, allowing users to describe what they need while Ordo builds and executes the necessary data-handling steps. A built-in audit trail records all signing and record-lifecycle events immutably, supporting compliance with GLP, GMP, 21 CFR Part 11, and EU GMP Annex 11 requirements.
Target Audience
Primary customers are bioanalytical CROs running immunoassays and LC-MS/MS, pharma and biotech manufacturing quality teams handling batch release and method validation, and regulated testing labs in food, water, and environmental sectors working under ISO 17025.
Features
- Auto-fills study reports directly from live data streams across instruments, LIMS, and spreadsheets without manual retyping
- Links every report value to its original source file (e.g., Study_Diary.pdf, p.4) for full traceability
- Natural-language data agent that builds and executes data-processing steps safely from user plain-word instructions
- Immutable audit trail capturing draft generation, review, and approval timestamps for every record-lifecycle event
- Supports GLP (21 CFR Part 58, OECD), GMP (Annex 11, 21 CFR Part 11), and ISO/IEC 17025 workflows across bioanalytical, pharma manufacturing, and regulated testing labs
- Compatibility with existing laboratory templates, filling 7 of 9 sections on average during study runs