IQVIA announced the launch of IQVIA RIM Smart, the first fully integrated, cloud-based, end-to-end regulatory information management solution for life sciences. Designed to leverage artificial intelligence (AI) and machine learning (ML), IQVIA Technologies’ new solution enables intelligent management of a product portfolio’s complete regulatory lifecycle.
“Life sciences companies are challenged by an increasingly complex, rapidly changing global regulatory environment within challenging financial constraints,” said Tal Rosenberg, senior vice president, Global Technology Solutions for IQVIA. “IQVIA RIM Smart is a technology-led solution for increasing speed, collaboration between functions, efficiency, and visibility across the full product portfolio, while also improving compliance performance.”
RIM Smart automates high-volume tasks, efficiently boosting accuracy, improving data quality, and reducing costs. This solution incorporates up-to-date regulatory intelligence information through the software, providing specific and detailed country-level regulatory requirements. Using an array of fully integrated modules that can be customized to meet specific customer needs, RIM Smart is appropriate for companies of all sizes.
“Built for regulatory professionals by regulatory professionals, RIM Smart will seamlessly integrate with IQVIA Technologies’ safety and quality compliance solutions. A range of open integration options gives customers the flexibility to plug and play, leveraging existing IT investments,” said Joe Rymsza, vice president, Pharmacovigilance and Regulatory Technology Solutions at IQVIA. “Delivered securely in the cloud and using proprietary AI and ML algorithms, IQVIA RIM Smart will provide interconnected, comprehensive and intelligent management of the entire regulatory process.”
RIM Smart will provide content management, registration tracking, monitoring of health authority interactions and commitments, submission planning, publishing, and soon, product labeling and translation capabilities. It handles routine workflows, enabling clients to use their resources to focus on bringing safe and effective products to market and ultimately driving healthcare forward.