QA Stack is a pharmaceutical technology company helping regulated manufacturers digitize and connect quality, manufacturing, laboratory, and compliance operations.

We provide both standalone and fully integrated solutions including Quality Management System (QMS), Electronic Batch Manufacturing Records (eBMR), Document Management System (DMS), Laboratory Information Management System (LIMS), CAPA Management, Deviations, Change Control, Audit Management, Training Management, Supplier Quality Management, Validation, and other GxP-critical processes.

Unlike traditional software vendors, we work closely with organizations to customize workflows, forms, approvals, reports, and integrations according to their operational and compliance requirements. Our platform is designed to support pharmaceutical, biotech, nutraceutical, and life sciences companies seeking scalable digital transformation while maintaining regulatory compliance.

Built with compliance at its core, QA Stack supports industry standards and regulatory expectations including 21 CFR Part 11, GAMP 5, ALCOA+, Data Integrity, GMP, and Annex 11 principles.

Our mission is to eliminate disconnected systems, manual processes, and spreadsheet-driven operations by providing a connected digital ecosystem that improves visibility, traceability, efficiency, and compliance across the enterprise.

QA Stack

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QA Stack

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