Transcription of ICH, WHO AND SUPAC GUIDELINES
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ICH, WHO AND SUPAC GUIDELINES
ICH, WHO AND SUPAC . GUIDELINES . ICH GUIDELINES . INTRODUCTION: The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) is a unique project that brings together the regulatory authorities of Europe, Japan and the United States and experts from the pharmaceutical industry in the three regions to discuss scientific and technical aspects of product registration. The purpose is to make recommendations on ways to achieve greater harmonisation in the interpretation and application of technical GUIDELINES and requirements for product registration in order to reduce or obviate the need to duplicate the testing carried out during the research and development of new medicines.
ICH is administered by the ICH Steering Committee which is supported by the ICH Secretariat. The ICH Steering Committee (SC) was established in April 1990, when ICH was initiated. The Steering Committee, working with the ICH Terms of Reference, determines the policies and procedures for ICH, selects topics for
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