From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.


The IQVIA Quality Management and Regulatory Suite integrates Quality Management System (QMS) and Registration Information Management (RIM) capabilities to streamline quality assurance and regulatory affairs for the life sciences sector. It offers AI-driven automation, end-to-end visibility, and real-time regulatory intelligence to enhance productivity, reduce time to market, and ensure compliance. Key components include the award-winning SmartSolve® eQMS, RIM Smart, and Regulatory Intelligence platforms.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Outdated compliance practices aren't viable amid evolving market and regulatory changes. IQVIA’s award-winning, end-to-end quality management system streamlines the product value chain, accelerates market entry, safeguards companies and patient safety, and meets complex regulatory demands.
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.