With the EMA’s Product Master Data Service live since 2024, ISO IDMP conformance is no longer looming at the horizon but an urgent regulatory imperative. Yet aligning complex medicinal product data to IDMP standards remains a major challenge for many Marketing Authorization Holders (MAHs).
Join experts from ACCURIDS and MAIN5 to discover a proven, data quality-driven method to assess and boost IDMP conformance using the IDMP Ontology. Learn how to automate maturity assessments, resolve common data issues, and rapidly build high-quality IDMP knowledge graphs. We’ll explore how AI supports intelligent data alignment across substances, products, and terminologies, and provide concrete examples of conformance measurement and remediation. This webinar is your practical guide to turning regulatory requirements into achievable data quality objectives — and ensuring your organization is ready for IDMP 2025 and beyond.
Agenda
- Overview of latest IDMP timelines and actions for MAHs
- Summary of pharma challenges in medicinal product data management
- Why product data conformance with ISO IDMP is a MUST-Have?
- Measure and increase IDMP data conformance with the IDMP Ontology and AI
- The investment case for data standardization with the IDMP Ontology
Speakers
- Raphael Sergent, ACCURIDS
- Michiel Stam, MAIN5
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