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EU Guide On Drug Pack Safety Features Updated Ahead Of Feb. 9 Deadline

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Executive Summary

With around two weeks to go for drug manufacturers to start complying with provisions of the EU Falsified Medicines Directive on affixing safety features on the packaging of  their medicinal products, the European Commission has issued updated guidance on the topic.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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