Rimsys announced a strategic partnership with Clarivate, a global leader in providing trusted information and insights to accelerate the pace of innovation. The new partnership pairs Clarivate Cortellis Regulatory Intelligence™ with the Rimsys RIM Platform, creating a new and unique solution that allows MedTech regulatory affairs professionals to access global regulatory information and harness it directly within automated workflows. The solution enables regulatory affairs professionals to access over 200,000 regulatory documents from more than 80 countries directly in the Rimsys platform and associate them at the individual product level to simplify market submissions and respond rapidly to regulatory changes. The Rimsys RIM Platform is a cloud-based software solution that is designed explicitly around MedTech regulatory activities and processes. It provides an integrated data hub for all regulatory information and documents and helps regulatory affairs teams streamline and automate critical processes. Rimsys Advanced Regulatory Intelligence allows MedTech regulatory affairs teams to: Identify market entrance requirements and historical product approval data to inform regulatory strategy. Associate relevant market regulations directly with product registrations and essential principles/GSPR tables. Automate regulatory product and UDI submissions with digital authoring, approval workflows, and publishing. Monitor changing laws, regulations, and guidance documents to identify affected products and avoid compliance issues.