Regulatory Planning & Tracking
RIMExpert™ addresses regulatory planning, tracking and data management by managing the global roll out plans and automating the creation of regulatory applications, activities and medicinal products, RIMExpert™ reduces data entry needs, improving data quality and increasing global oversight and control.
Benefits
Standardized Processes
Standardize regulatory planning, tracking and registration management processes
Collaboration
Strengthen collaboration between headquarter(s) and affiliates
Single Workplace
Create one common place to work in all registration activities
Full Control
Control registration activities throughout the lifecycle of the product keeping abreast of timelines and status of commitments and agency questions
Efficiency
Synchronize efforts for maximum efficiency of enterprise regulatory resources
Centralization
Having one access point to all activities, questions, commitments, correspondence and authorizations for every application
RIMExpert™ Features
- Tracking registrations, content and other meta-information
- Interactive dashboards for actionable regulatory activities and registrations overview
- Codifying and maintaining country specific requirements and regional regulatory knowledge
- Planning global and local regulatory activities (e.g. submissions, commitments, correspondence etc.)
- Support for the IDMP target operating model
Related Content
Get IDMP ready by joining our IDMP journey
Discover our Life Sciences solutions
Connect with us today!