IQVIA RIM Smart. Intelligence, automation and integration.
Evolving global regulatory requirements are becoming more complex and placing an ever-greater burden on drug and medical device manufacturers. To meet those requirements and demonstrate that products are safe and effective, the quality, regulatory and compliance functions are essential—yet all too often they reside in organizational silos. By breaking down those silos and enabling better communication and collaboration, life sciences organizations can pave the way for a connected compliance ecosystem that leads to shorter development cycles, lower operational costs, while minimizing compliance-related risks.
IQVIA RIM Smart. Intelligence, automation and integration.
Boost your regulatory productivity.
Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.