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


This white paper explores how AI‑enabled regulatory information management (RIM) helps life sciences organizations accelerate global market access while maintaining compliance. Drawing on expert insights from regulatory leaders at Dentsply Sirona, Cynosure Lutronic, and IQVIA, it examines global regulatory complexity, resistance to digital transformation, and the role of AI in streamlining submissions, registrations, and lifecycle management. Learn how modern RIM solutions, including IQVIA SmartSolve RIM, enable more efficient, connected, and resilient regulatory operations across regions.
SmartSolve® RIM manages regulatory submissions, product registrations, and health authority interactions.
Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
IQVIA SmartSolve® Fundamentals is a cloud‑based QMS designed for Small Medtech and Pharma EBP. It automates CAPA, Deviation, Document, and Change Management, helping lean teams stay compliant while minimizing IT burden.