Core LIMS
Know where every sample is — and who held it
Aureon LIMS sample management covers accessioning, storage hierarchy, chain of custody, aliquots and lineage, and disposition. Lab managers see location and workload; QA sees an attributable custody history.
The problem
Why this matters on the bench
When samples live in spreadsheets, shared drives, and verbal hand-offs, location is uncertain and custody breaks under inspection. Aliquots lose their parent, storage maps drift, and disposition is a memory exercise.
Capabilities
How it works
Sample management, step by step
Accession with identity
Register samples with identifiers, source, received condition, and required tests — attributable from the first scan.
Place in a real hierarchy
Store against sites, rooms, units, shelves, and boxes so location is a controlled field, not a note.
Move with custody
Transfers record who, when, from, and to. Custody is a lifecycle, not a comment log.
Split with lineage
Aliquots and derived samples keep parent-child relationships so results can be traced to origin.
Dispose with a record
Disposition closes the lifecycle. Regulated records are not hard-deleted.
Regulatory relevance
Compliance, precisely stated
Sample identity and custody history are foundational to 21 CFR Part 11 record integrity and ISO/IEC 17025 sample-handling expectations. Aureon is designed to support those workflows; laboratories remain responsible for validation in their quality system.
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.
Questions
What evaluators ask
Yes. Derived samples inherit lineage to the parent and carry their own custody events.
See sample management against your SOPs
Book a demo or talk to sales about scope and validation support.