Veeva Vault RIM is not the only option for Regulatory Information Management (RIM) Systems. Explore other competing options and alternatives. Other important factors to consider when researching alternatives to Veeva Vault RIM include performance and training. The best overall Veeva Vault RIM alternative is Clinical Research Suite. Other similar apps like Veeva Vault RIM are Kivo, RegDesk, Rimsys, and AmpleLogic Regulatory Information Management System (RIMS). Veeva Vault RIM alternatives can be found in Regulatory Information Management (RIM) Systems but may also be in Clinical Trial Management Systems.
Research Manager supports researchers and organisations in preparing, executing and administering (clinical) research data. Our expertise is the collection, validation and enrichment of data. With Research Manager, we offer a research platform that allows researchers to have all functionalities and information in one place and to share it with each other. The platform facilitates researchers who want to be prepared for a future where the patient, access to data, and sharing data are key.
Kivo makes simple and affordable document management systems including RIM, eTMF, and QMS. A single license grants access to all our solutions, so you can supercharge cross-functional collaboration without breaking the bank. Fully validated, Part 11 and SOC 2 compliant, Kivo is designed forGxP.
RIMSYS Regulatory Management Software is built for and by regulatory affairs professionals and specifically designed for the medical device and in-vitro diagnostic (IVD) industry. By offering an intuitive collaboration hub, medical device companies can now actively navigate the rapidly changing regulatory landscape. RIMSYS offers a suite of cloud-based regulatory affairs software solutions for the medical device and IVD industry to manage global product registrations, standards, essential principles, regulatory documents, regulatory intelligence and more.
RIMS (Regulatory Information Management System) allows companies to team up, preserve application information data from various locations and enhance the processes of preparing a submission, as well as simplify the publishing and tracking of all regulatory activities that support a product’s complete life cycle.