Blog Archive: Rimsys Updates

Rimsys joins MedTech Europe

This week Rimsys became an associate member of MedTech Europe, the European trade association representing the medtech industry. As a member of the organization, we’ll have visibility into regulatory changes across the region as they’re being formed, and the opportunity to shape how those regulations are implemented.

Better Together: Regulatory Intelligence and Regulatory Information Management

Today we announced a new partnership with Clarivate to bring together regulatory intelligence from Clarivate Cortellis with regulatory information management from the Rimsys Platform. This combined offering will allow RA professionals to access 200k+ regulatory documents from over 80 countries, and harness insights directly in automated processes.

Arena Solutions and Rimsys Announce Partnership to Offer an End-to-End Quality and Product-Centric Regulatory Solution

Arena Solutions, a leader providing cloud-based product development solutions for high tech, consumer electronics, and medical device industries, today announced a new partnership with Rimsys Inc., a world-leading provider of a holistic Regulatory Information Management (RIM) software platform designed specifically for medical technology (MedTech).

Rimsys Releases New Automated Unique Device Identification (UDI) Module for Its Holistic MedTech RIM Platform

Rimsys, a world-leading Regulatory Information Management (RIM) software platform for medical technology companies, announced a new brand identity and tagline. Rimsys, the only holistic RIM software on the market designed specifically for medical technology companies, with functionality for the pillars of regulatory affairs, rebranded to accurately

Rimsys named 2020 Top Technology Company Finalist by Tech 50 Awards

Rimsys, a world-leading Regulatory Information Management (RIM) software platform for medical technology companies, named 2020 technology company finalist.

The Ultimate Guide to the EU MDR General Safety and Performance Requirements (GSPR)

With the European Medical Device Regulation (MDR) looming, medical device companies are focusing on ensuring compliance with the new regulations. One of those key aspects of compliance is to ensure your devices conform to the General Safety and Performance Requirements (GSPR). This guide provides you with some practical guidance on how to meet th