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.
You'll learn:
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The seven KPIs to measure RIM results
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How GE saved ~200 hours of reporting work per year
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Best practices for affiliate activity, health authority approvals, and submission rejections
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How to achieve a "single source of truth"
James is Head of Regulatory Operations at GE Healthcare. He has 19 years 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).
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