Regulatory Information Management System
RIMS (Regulatory Information Management System) is a web-based solution that helps life sciences companies to collaborate, manages global applications information data, Tracking the regulatory communications as well as customer communications and status of the regulatory activities that support entire product life cycle process.
ANDA tracker allows you to manage the complete Lifecycle of Applications filed against regulatory.
DMF (Drug Master File) submissions can be managed until the closure with early alarms on commitment dates.
BENEFITS OF RIMS
Streamlines the submission process
Improve collaboration & Accuracy
Ensure compliance risks
Eliminate the wastage
Reduce the costs
Increases the efficiency
Centralized Database can be accessed from regardless of location
Features of RIMS
Tracks the Customer Communications
Tracks the regulatory communications
Tracking of Approvals/rejection
Tracks all the QMS related activities
Identify the product registration details