IQVIA’s SmartSolve® RIM helps life sciences organizations simplify global regulatory affairs by replacing fragmented systems with a unified, AI-enabled platform. The solution centralizes regulatory submissions, product registrations, eCTD dossiers, labeling, and health authority interactions, creating a single source of truth across global markets. By improving data integrity, workflow traceability, and visibility into submissions and regulatory commitments, SmartSolve® RIM reduces compliance risks and strengthens inspection readiness. The platform also supports faster execution of regulatory activities—from IND/CTA submissions through post-approval variations—while helping organizations adapt to evolving global requirements such as IDMP/SPOR, ultimately improving operational efficiency, r

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