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EU calls on stakeholders to join task force on new ID standards for medicines

This article was originally published in SRA

Executive Summary

An EU task force is to be set up to discuss how new standards for the identification of medicinal products (IDMP) are to be implemented1. The European Medicines Agency, which wants industry and other stakeholders to be part of the task force, says the aim is to open a dialogue with all interested parties to discuss the implementation of the new ISO IDMP standards from July 2016.

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