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Standards we work to: GAMP 5, FDA 21 CFR Part 11, EU Annex 11, ALCOA+ Data Integrity, PIC/S Guidance, ISO 9001:2015, EudraLex Vol 4, Validation Master Plan, Risk-Based · FMEA, CSA · Software Assurance, Audit-Ready Documentation, SDLC

Column Management

Every column,accounted for.

Chromatography columns are consumables that carry your data integrity. Built for pharma API QC laboratories, Column Management gives every column a controlled record from receipt to destruction — issuance, system-suitability history and a full audit trail — so a column is never the reason a result gets questioned.

At a glance

Make every column decision traceable

Column Management · Lab QC-2● LIVE
C18-204
72%
of limit

In use

HILIC-118
41%
of limit

In use

C8-052
96%
of limit

Retire soon

Column efficiency (plates) · last 7 checks

When an analyst can't say how many injections a column has seen, or whether its efficiency has drifted, every result it produced is open to challenge. Column Management removes that doubt.

Usage, system-suitability trends and full history live against each column, so lab managers make retire-or-keep calls on data — and inspectors see a complete lineage.

Illustrative system-suitability performance trend across a column's lifecycle

Why it matters

Made for regulated QC labs

The whole lifecycle, one record

From the day a column arrives to the day it's retired, every step lives on a single controlled record — nothing tracked in a spreadsheet on the side.

Data integrity you can show

Access-controlled and fully audit-trailed, so an inspector sees a complete, defensible history for every column in the lab.

No column left in question

Always know a column's status, history and whereabouts — so a column is never the reason a result gets challenged.

Next step

Bring your columns onto the record.

We will map your current column-tracking process and show how it looks in Column Management — access-controlled, with a full audit trail from receipt to destruction.