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For over 17 years, Quantum Analytical Data Systems has been the trusted technology partner for pharmaceutical manufacturers worldwide, helping them navigate the complex intersection of innovation, compliance, and operational excellence.
Founded in 2008 by a visionary team of software engineers, we’ve grown from a startup in Pune—India’s thriving tech hub—into a global leader serving pharmaceutical companies. Our mission remains unchanged: to empower pharmaceutical manufacturers to digitize, integrate, and elevate their operations while maintaining the highest standards of quality and compliance.
Our integrated suite of solutions creates a seamless data continuum from laboratory to boardroom:
QUADS ERP delivers comprehensive enterprise resource planning designed specifically for regulated manufacturing environments, ensuring every process meets stringent pharmaceutical standards.
Warehouse Management System (WMS) provides real-time inventory control and materials flow optimization, eliminating bottlenecks and ensuring supply chain reliability.
Laboratory Information Management System (LIMS) drives quality control and analytics with comprehensive testing workflows that accelerate decision-making while maintaining compliance.
Quality Management System (QMS) safeguards continuous improvement through robust compliance frameworks that exceed global regulatory requirements.
What sets Quantum apart is our unified architecture—every module shares the same foundation, ensuring consistent master data, single-source reporting, and dramatic improvements in both productivity and compliance readiness.
Industry Expertise That Runs Deep
Two decades of pharmaceutical manufacturing experience is embedded in every workflow, feature, and process we design. We don’t just understand software—we understand your business.
Engineering Excellence
Our award-winning development team combines rapid innovation with the security and reliability that pharmaceutical manufacturing demands. We iterate quickly while never compromising on quality.
Compliance-First Architecture
Every solution is built to exceed global regulatory standards including cGMP, USFDA 21 CFR Part 11, and EU Annex 11. Compliance isn’t an afterthought—it is our foundation.
Scalable for Growth
Whether you need cloud, on-premises, or hybrid deployments, our modular architecture grows with your business, from single facilities to global manufacturing networks.

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