IDMP Success Webinar
From Spreadsheets to IDMP-Ready in 6 Months
How one global pharma built a single source of truth for medicinal product data, and what your team can learn before IDMP becomes the standard worldwide.
ISO IDMP isn't a cosmetic update - it's a fundamental shift in how medicinal product data is defined, structured, and exchanged with regulators.
The data points required per product have jumped from around 60 to over 200, and health authorities across Europe, North America, and beyond are aligning to the same global standard.
For regulatory affairs teams still relying on Excel and disconnected systems, the gap between today's setup and tomorrow's submission requirements is widening fast.
In this 50-minute on-demand webinar, you'll learn:
- Why ISO IDMP demands a fundamentally different approach to product data
- How a 100-year-old pharma with presence in 70+ countries approached its RIM implementation
- The step-by-step process that delivered a working system in 6 months
- How to use validated master data sources for a clean, low-risk migration
- What "single source of truth" actually looks like in practice
- Practical advice from a regulatory affairs lead who's done it: the mistakes to avoid and what to prioritize first
- How to build a regulatory data foundation that's ready for evolving global requirements
Watch the full webinar now
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