The only pre-validated, pre-configured LIMS for Pharma and Biotech
Deploy quickly, work productively with LabVantage Pharma LIMS
Imagine the immense time and cost savings from being able to deploy a full end-to-end informatics solution for your R&D, analytical, QC manufacturing, and other labs where the critical validation of the software as delivered was already done for you.
LabVantage provides the world’s only pre-validated and pre-configured pharmaceutical LIMS, allowing you to save up to 85% in implementation costs and 75% in time compared to a traditional LIMS implementation. The out-of-the box functionality includes everything you need, from batch management, stability testing, and consumables management to environmental monitoring, barcode label printing, and more.
Highly flexible and robust, LabVantage Pharma LIMS scales and supports your organization, whether you are monitoring quality control for launching your first product or collecting stability data on multiple products. Advanced functionality, too, like predictive and prescriptive analytics, helps digitally transform your organization, so you can streamline processes, boost productivity, and leverage valuable scientific and business insights from your data.
Count on LabVantage Pharma for:
- Out-of-the-box fully operational and functional, pre-validated LIMS pre-configured with pharma and biotech templates and workflows
- Pre-validation in compliance with GAMP 5 guidelines
- Compliance with FDA 21 CFR Part 11, European Union’s EudraLex Annex 11, and other global regulations
- Rapid, reduced-risk deployment, ideal for labs with limited IT resources
- Embedded ELN, LES, and SDMS for managing day-to-day operations, research, and data management – no point solutions to knit together
- Deploy via validated SaaS (Enterprise and Standard options), cloud-hosted, or on-premise