Medtech leaders are challenged to present compelling ROI when implementing a Regulatory Information Management (RIM) system to prove success.
By consolidating 10+ sources of information into a single, connected system, GE found seven unique ways to measure how their RIM suite is helping achieve speed and compliance objectives.
Access these exclusive details to learn:
- The seven KPIs to measure RIM results
- How GE saved ~200 hours of work per year
- Best practices for affiliate activity, health authority approvals, and submission rejections
- How to achieve a "single source of truth"
Head of Regulatory Operations
James is the Head of Regulatory Operations at GE Healthcare. He has 19 years of experience in the industry, including 9 years at a major innovator, as well as stints in outsourcing, consulting, generic pharma and now nuclear medicine. Recent experience includes system and process design, migration, training and system ownership for a full Veeva RIM implementation (Registrations, Submissions, and Submissions Archive).