IQVIA’s RIM Smart Submission Management is a cloud-based solution streamlining regulatory product registration for pharma and medtech. It integrates dossier planning, publishing, validation, and dispatch in one platform, ensuring efficiency, transparency, and compliance with global standards like eCTD and NeeS. Features include global forecasting, automated content sequencing, embedded regulatory intelligence, and health authority interaction management. The system improves submission productivity, reduces approval timelines, and supports real-time regulatory updates. Built with deep industry expertise, it enables life sciences companies to accelerate product approvals, cut costs, and maintain compliance throughout the product lifecycle.

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