Pharma manufacturing can’t rely on spreadsheets or outdated systems. Manual processes slow batch release, increase compliance risks, and threaten product quality.
LabVantage Pharma LIMS is a purpose-built, pre-validated platform that helps manufacturers stay audit – ready, accelerate operations, and cut deployment costs by 85%. Go live in as little as 90 days with built-in compliance to FDA 21 CFR Part 11, EudraLex Annex 11, and global GxPs.
With automated workflows, instant Certificates of Analysis, and enterprise-grade security, LabVantage Pharma delivers confidence at every stage – from data integrity to batch release.
Simplify operations, strengthen compliance, and deliver safe, high – quality products – faster.
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