- Quality
- Manufacturing
Automated Batch Release QA
An agent workflow that cross-references batch records, CoA data, and SOPs to flag deviations before release — reducing manual review time by 60%.
The Problem
Batch release in pharma manufacturing involves reviewing dozens of documents across multiple systems: batch records, certificates of analysis, deviation logs, and SOPs. A single missed discrepancy can delay a release by days.
The Workflow
This example shows a Komposer workflow with three agents working in sequence:
- Data Collector — pulls the latest batch record from the MES and the corresponding CoA from the LIMS
- Deviation Checker — compares results against specification limits and flags out-of-spec values with supporting evidence
- Report Generator — drafts a release decision summary and routes it to the QA reviewer via email
Setup
Connect your MES and LIMS using the built-in integrations. Point the workflow at the batch number and let it run. The output is a structured report the reviewer can approve or escalate directly in their inbox.
Results
Teams using this workflow report a 60% reduction in manual review time and fewer release delays caused by overlooked documentation gaps.
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