Rimsys Regulatory Information Management Software is a platform designed to help MedTech companies streamline and centralize their regulatory affairs operations. Rimsys offers Regulatory Information Management (RIM) software that enables regulatory affairs teams to manage compliance processes more efficiently and confidently, reducing reliance on manual spreadsheets and disconnected tools.
The core function of Rimsys is to centralize regulatory data, automate submission processes, and provide comprehensive visibility into product registrations, expirations, standards, and regulations. The software supports the full spectrum of regulatory activities needed by medical technology organizations, including project management for regulatory submissions, tracking global product registrations, and monitoring compliance requirements and timelines.
By providing an integrated platform, Rimsys enables MedTech companies to:
- Plan regulatory projects more effectively
- Execute submissions and updates more quickly
- Ensure ongoing compliance with international standards and regulations
- Reduce the risk of non-compliance, product recalls, and missed expirations
Rimsys differentiates itself from traditional, spreadsheet-based approaches by offering automation, centralization, and real-time status tracking, which helps teams accelerate the delivery and increased availability of life-changing medical technologies.
Who Uses Rimsys Regulatory Information Management Software?
Rimsys primarily serves MedTech companies and regulatory affairs teams seeking to manage global compliance for a wide range of medical products. Notable customers include Omron, Siemens, Johnson & Johnson, Smith + Nephew, Terumo, Novartis, and Avanos, illustrating Rimsys's adoption among leading multinational healthcare and medical device organizations.
How Was Rimsys Started?
Rimsys was founded in 2017 in Pittsburgh, Pennsylvania, by regulatory affairs professionals James Gianoutsos (Founder & CEO) and Brad Ryba (Co-Founder & Board Member). Their direct experience in the medical technology industry informed the development of a solution specifically tailored to the complex regulatory needs of MedTech companies.
You can learn more about the company background and team on their About page.
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