What does ICH mean in English?

The International Conference on Harmonization of Technical Requirements for Pharmaceuticals for Human Use ( ich is an international organization created by representatives from the U.S., European Union and Japan. It was established to develop and periodically update harmonized technical requirements for the conduct of non-clinical studies and for the submission of dossiers to regulatory authorities worldwide.

What does ICH mean in Hebrew?

The Hebrew acronym for the International Organization for standardization (or the acronym used in the Hebrew language), ICH, is the title of the standard for written documentation in the health and life sciences that applies to all aspects of pre-clinical and clinical trials. The standard applies to all documentation related to studies and tests that use investigational drugs or medical devices (including biological products, radiopharmaceuticals, and surgical implants), and the documentation of the results of these tests.

What does ICH mean in French?

ICH is an acronym for International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use, a European organization. The organization exists to develop common technical standards for the evaluation and licensing of new drugs and medical devices.

What does ICH mean in Spanish?

The ICH system stands for International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The ICH program was created to help streamline drug development processes to reduce costs and time. It was established in 1997 by the Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Council for International Organizations of Medical Sciences (CIOS).

What does the ICH mean in English?

The ICH is an acronym for the International Conference on Harmonisation. It is an organization made up of representatives from the European Union, Japan, the United States, Canada, and other countries who work to develop and maintain harmonized guidelines for drug manufacture, packaging and labelling, and for the preclinical testing of new drugs.