Industry solution
LIMS for pharmaceutical QC — from accession to lot release
Pharmaceutical QC labs need throughput without losing the trail. Aureon LIMS is built for sample lifecycle, method and specification control, QC/OOS/CAPA, and CoA — designed to support 21 CFR Part 11 workflows.
Industry pains
What slows labs like yours down
Release waits on reconstruction
When results, deviations, and CoA live in different tools, lot release becomes a scavenger hunt.
Inspection asks for the trail
QA needs attributable history and signatures — not a folder of PDFs assembled the night before.
Methods drift
Specification versions used at test time must match what appears on the certificate.
Relevant modules
- Sample Management & Chain of Custody
- Test, Method & Specification Management
- Quality Control & SPC
- Deviation / OOS / CAPA
- Audit Trail & 21 CFR Part 11 Compliance
- Batch & Lot Release
- Reporting & Certificate of Analysis (CoA)
- Stability Management
Outcomes we aim for
- Faster path from last result to release documentation
- Fewer findings rooted in missing custody or unsigned changes
- Clearer specification versioning on reported results
We do not publish invented time-savings or finding-reduction percentages.
Questions
Answers for your evaluation team
It is the laboratory system of record for samples, tests, QC, and lab-originated quality events. Enterprise QMS integration is discussed during discovery.
Map this industry story to your sites
Demo and quote conversations start from your methods, not a generic deck.