10 Small Submissions
No more than 10 Documents per submission
RIM signifies Regulatory Information Management. It is an integrated software platform that streamlines the Regulatory industry's product application and registration lifecycle tracking. It enables end-to-end tracking of Regulatory activities related to various products like Pharmaceuticals, Biologics, and Cosmetics, etc. With time, submission management practice in the Regulatory space has become comprehensive and interesting. A robust RIMS system can help to organize the work involved throughout the lifespan of product development and medicine marketing.
RIMS improves Regulatory industry development and coordinates the product registration process to track and manage all Regulatory activities and life cycles. It also avoids replicated effort and simplifies product applications and submission operations. In brief, to avoid labor intensive upkeep, RIMS came into existence. A universal approach to Regulatory management. Freyr RIM solution is the advanced Regulatory information management tool focussed on boosting speed, cooperation, competence, and outlook around your whole international portfolio, improving performance at a lower cost.