A comprehensive, audit-ready LIMS solution designed specifically for small and medium pharmaceutical manufacturers to streamline operations across Quality Control, Quality Assurance, Production, R&D, Inventory, and Compliance—from sales order to finished goods dispatch.
LIMS helps pharma manufacturers manage QC, QA, BMR, inventory, deviations, and dispatch in one easy system — ready for WHO-GMP, 21 CFR Part 11 and Schedule M inspections.
Perform in-process quality checks during production, log deviations immediately, and maintain real-time batch quality status.
Perform in-process quality checks during production, log deviations immediately, and maintain real-time batch quality status.
Execute comprehensive final product testing, analyze results against specifications, and provide release recommendations.
Review all testing data, approve final batch release, and generate Certificates of Analysis (COA) for customer shipment.
Comprehensive system for logging deviations, conducting root cause analysis, and tracking Corrective and Preventive Actions (CAPA) through closure with automated notifications and escalations.
Ready to take your business to the next level? Contact us today and let's get started!
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