The purpose of ICH is to make recommendations on ways to achieve greater harmonization 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.

To provide a unified standard for the European UNION (EU), Japan and the United States to FACILITATE the mutual ACCEPTANCE of clinical data by the regulatory authorities in these jurisdictions

The purpose of ICH is to make recommendations on ways to achieve greater harmonization 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.

To provide a unified standard for the European Union (EU), Japan and the United States to facilitate the mutual acceptance of clinical data by the regulatory authorities in these jurisdictions