CENTRALIZE YOUR REGULATORY INFORMATION.
Get a clear picture for the planning and scheduling of your business resources and regulatory processes.
DRIVE HARMONIZATION; ENSURE COMPLIANCE.
Save time and effort with single data entry. ISO IDMP-ready.
PLAN, TRACK, AND REPORT BETTER AND FASTER.
Easy data search and reporting. Easy access to real-time information.
RIMExpert is a powerful business intelligence tool designed to standardize the data management process across your entire company and over the entire life cycle of your products. No double data entry. No extra effort. No wasted time.
To improve the performance and efficiency of business processes, your regulatory affairs group and strategic marketing management teams must have a clear picture of the products statuses within the marketing authorization process. With RIMExpert, the answers you need are always in-hand.
After processing, organizing, and structuring your data, RIMExpert presents it via a configurable output interface that integrates with your existing reporting formats, including dashboards, tables, and exportable dynamic reports. This provides your regulatory affairs department, executive management, and other stakeholders with a complete, real-time overview of current information and upcoming activities. Your teams will be able to better plan and schedule for optimal product life cycle management.
PRODUCT PORTFOLIO PLANNING AND REPORTING
PLANNING, TRACKING, AND REPORTING
OF REGULATORY ACTIVITIES
IN-PROCESS METADATA MONITORING
ON-DEMAND REPORTING WITH PREDETERMINED
CONTENT AND AUTOMATIC DISTRIBUTION
DATA DEFINITION IN ACCORDANCE WITH
XEVMPD AND ISO IDMP DATA MODELS
AUTOMATIC GENERATION OF DIFFERENT DOSSIER STRUCTURES (CTD, ACTD, COUNTRY-SPECIFIC, MEDICAL DEVICE DOSSIERS, ETC.), WHICH CAN BE PUBLISHED IN DIFFERENT FORMATS (ECTD, NEES, PDF/PAPER, ETC.)
SEAMLESS INTEGRATION INTO
THE REGULATORY PROCESSES
SECURE ACCESS BASED ON
PRE-CONFIGURED AND VALIDATION-READY