Knowledge Brief: Overview, Regulatory Framework, EMEA

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By Dr. Kate McCormick
Level: Fundamental

This Knowledge Brief provides a basic overview of the EMEA's organizational structure, responsibilities, and regulations relevant to the manufacture of medicinal products.

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Last Update: 14 September 2011

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Knowledge Briefs are developed from a wide variety of resources including ISPE training courses, conferences, seminars, technical documents, individual authors who are subject matter experts, as well as expert interchanges within the Society's Communities of Practice.