Core LIMS
Get instrument data in — and keep transcription out
Aureon LIMS is designed to receive instrument results into controlled records so analysts spend less time retyping values and QA spends less time questioning provenance.
The problem
Why this matters on the bench
Manual transcription is slow and hard to defend. When a value is typed from a printout, the chain from instrument file to reported result is a narrative, not a record.
Capabilities
How it works
Instrument integration, step by step
Identify the instrument
Instruments are controlled records — identity, status, and (where used) calibration context.
Map the result
Result fields map to tests and specifications so inbound data lands in the right method context.
Review before use
Imported values follow review and approval rules. Integration does not bypass signatures.
Keep the trail
Source context stays with the result so CoA and audit export can show how the number arrived.
Regulatory relevance
Compliance, precisely stated
Data integrity guidance expects attributable, original (or true-copy) records. Integration is designed to reduce informal transcription; validation of each interface remains a customer responsibility.
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
No. Interfaces are scoped. Core LIMS is designed for structured capture; specific drivers and CDS links are planned with your lab.
See instrument integration against your SOPs
Book a demo or talk to sales about scope and validation support.