SmartSolve® Deviation Management

SmartSolve® Deviation Management streamlines the identification, investigation, and resolution of deviations for pharmaceutical organizations, ensuring product quality and regulatory compliance. The platform offers closed-loop workflows, risk assessment, analytics, and seamless integration with over 20 quality modules, including CAPA, NC, and Change Management. Powered by AI and Microsoft Azure, SmartSolve enables faster cycle times, proactive risk management, and continuous improvement across the value chain.

SmartSolve® eQMS for Pharma

Explore how SmartSolve® eQMS for Pharma, an award-winning enterprise quality management system, seamlessly integrates quality into every aspect of life sciences operations. It empowers organizations to elevate quality standards, ensure regulatory compliance, accelerate time-to-market, and manage risks effectively.

SmartSolve® Fundamentals for EBP

IQVIA SmartSolve® Fundamentals is a cloud-based QMS for small biopharma companies. It automates CAPA, Deviation, Document, and Change Management to ensure compliance with minimal IT resources.

SmartSolve RIM

SmartSolve® RIM manages regulatory submissions, product registrations, and health authority interactions.

SmartSolve® eQMS for MedTech

Discover how an end-to-end eQMS solution empowers QARA professionals to remain agile, well-informed, and proactive in ensuring the safety and efficacy of medical devices.

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Robust Audit Programs

IQVIA SmartSolve® CAPA Management

SmartSolve® Supplier Management

SmartSolve® Change Management

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