Quality expansion
Lots, expiry, and usage against the work that consumed them
Track reagents and consumables so methods can show what was used — and expired material is harder to apply quietly.
The problem
Why this matters on the bench
When inventory is a closet spreadsheet, expired lots still reach the bench and usage cannot be reconstructed.
Capabilities
How it works
Inventory, step by step
Receive lots
Identity, expiry, and storage are recorded at receipt.
Issue to work
Usage can be associated with tests or methods.
Control status
Quarantine, release, and expiry statuses are visible to the bench.
Regulatory relevance
Compliance, precisely stated
Material control supports data integrity and ISO/IEC 17025 resource requirements.
Aureon LIMS is designed to support 21 CFR Part 11 and ISO/IEC 17025 workflows. It is not FDA-approved or “Part 11 certified.” Customers remain responsible for system validation, SOP alignment, and regulatory interpretation in their own quality system.
Related modules
Questions
What evaluators ask
Instruments have their own registry. Inventory focuses on reagents and consumables.
See inventory against your SOPs
Book a demo or talk to sales about scope and validation support.