LIMS Implementation for a Leading Pharma QC Lab
Client: Confidential Pharma Client
The Challenge
Manual sample tracking and paper-based QC workflows leading to audit findings and delayed batch release.
Our Solution
End-to-end LabVantage LIMS implementation with 21 CFR Part 11 validation, instrument integration, and electronic batch records.
Key Outcomes
- 60% reduction in quality audit preparation time
- Automated sample chain-of-custody for 200+ daily samples
- Full 21 CFR Part 11 compliance achieved in 12 weeks
- Zero critical audit findings post-implementation
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