Quality expansion
Stability pulls you can schedule — and defend
Plan protocols, conditions, and time points so stability work is a controlled program, not a calendar reminder and a shared folder.
The problem
Why this matters on the bench
Missed pulls, unclear chamber assignments, and results that do not point back to a protocol make stability programs fragile under review.
Capabilities
How it works
Stability, step by step
Define the protocol
Conditions, time points, and tests are versioned with the study.
Place and pull
Inventory locations and pull events are recorded against the protocol.
Test and trend
Results attach to time points so trends are visible without a side spreadsheet.
Regulatory relevance
Compliance, precisely stated
Stability programs are commonly inspected in pharmaceutical QC. Aureon is designed to keep protocol, pull, and result together.
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
Stability is a quality expansion module. Many QC labs add it after core sample-to-result is live.
See stability against your SOPs
Book a demo or talk to sales about scope and validation support.