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Unlocking the Potential of IDMP for Global Exchange of Medicinal Products Data
Session Chair(s)
Malin Kristina Fladvad, PhD, MSc
Portfolio Officer
Uppsala Monitoring Centre, Sweden
This session will discuss how the ISO IDMP standards have a pivotal role in enhancing global pharmacovigilance and improving visibility in the product supply chain. The collaborative efforts of the Global IDMP Working Group reflect the need to advance this critical endeavor.
Learning Objective : Define IDMP standards and explain their benefits when globally implemented; Describe the role of the unique global IDMP identifiers in data exchange of medicinal product information; Discuss the impact of global IDMP identifiers on different use cases in the medicinal product life cycle, for example, pharmacovigilance and drug shortages, supply chain integrity.
Speaker(s)
US FDA Policy on Identification of Medicinal Products (IDMP): Global Framework for IDMP Implementation
Ron Fitzmartin, PhD, MBA
FDA, United States
Senior Advisor, Office of Regulatory Operations, CBER
Unlocking the Potential of IDMP for Global Exchange of Medicinal Products Data
Hilmar Hamann, PhD
European Medicines Agency, Netherlands
Head of Information Management
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