OpenRIMS

What is OpenRIMS-RP OpenRIMS-RP, short for Regulatory Processes, is an open-source web-based workflow design module developed by OpenRIMS to assist National Medicines Regulatory Authorities (NMRA) in digitizing and automating their work processes. These processes can include medicines registration, pharmacy registration, inspections, import/export licensing, and clinical trial applications. It builds on the success of Pharmadex, an R-IMS solution created by the USAID-funded SIAPS Program implemented by Management Sciences for Health. What are the characteristics of OpenRIMS-RP OpenRIMS-RP is characterized by its adaptability to different countries and contexts, making it a digital public good. It adheres to the Digital Public Good Principles and supports the Principles for Digital Development. By aligning with international standards, OpenRIMS-RP ensures a seamless integration of best practices into technology-enabled programs. Designed as an open source solution, it allows for customization and collaboration, making it an effective tool for NMRA digitalization and automation. What are the application scenarios of OpenRIMS-RP OpenRIMS-RP is primarily applied in regulatory processes within NMRA, such as medicines registration, pharmacy registration, inspections, import/export licensing, and clinical trial applications. It enables the digitalization and automation of these processes, improving efficiency and transparency in regulatory work. For instance, it can facilitate the registration of new medicines, streamline inspection procedures, and automate import/export licensing, ensuring that regulatory activities are conducted in a timely and compliant manner.