The IDMP standards aim to harmonise how pharmaceutical products and substances are described globally. But how will that benefit patients and who will make sure the standards are properly implemented? Uppsala Monitoring Centre’s Malin Fladvad and Olle Lagerlund discuss the advantages and challenges of this global standardisation effort in the Drug Safety Matters podcast.
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23-25 October: Global Pharmaceutical Regulatory Affairs Summit
From 23-25 October 2023, UNICOM will present the results of work package 2 related to substances. For more details, see the UNICOM website.
UNICOM Gap Analysis on existing and new standards and profiles – UNICOM presentation for EFPIA PVEG WG
Work package 1 focuses on IDMP-related standards and terminologies, identifying gaps in existing standards and the need for new ones.