Quality Control — Chemical Pharma ERP
Run QC/QA workflows, COA generation, stability testing and sample management with full traceability.
Request a Demo →From sample to certified release
In regulated manufacturing, nothing ships without QC. Samples must be logged and tested against specs, results reviewed and approved, stability programmes run over months, and a certificate of analysis produced — all traceable and defensible.
This module runs QC/QA end to end: sample login and testing, specification-based results, COA generation, and stability study management — so release decisions are made on complete, traceable data.
It connects directly to the rest of your Chemical Pharma ERP, and can be extended with AI or mobile apps for field teams.
What the module handles
The QC lab, connected to release
How it works
From sample login to COA and release.
What it changes for your business
Other modules in the Chemical Pharma ERP
One integrated system
Who it is for
Manufacturers with a regulated QC lab:
Quality Control — frequently asked questions
Does it manage samples and testing?
Yes. Samples are logged, labelled and tracked through spec-based testing, with results reviewed and approved before any release decision is made.
Can it generate certificates of analysis?
It can. On approval of results, a COA is generated and tied to the specific lot, so customers and auditors get defensible proof of quality.
Does it handle stability studies?
It does. Stability programmes are scheduled and tracked over their full duration, with pull points and results recorded against the study.
Are results traceable to the lot?
Yes. Every QC result is linked to its lot and batch, giving the traceability needed for release, audits and any later investigation.
See Quality Control in your Chemical Pharma ERP
See Quality Control connect your lab to compliant release — book a demo aligned to your QC workflows.
Request a Demo →