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A list of all pages that have property "Why is this important?" with value "ICH’s mission has been embodied in its Articles of Association as follows: * To make recommendations towards achieving greater harmonisation in the interpretation and application of technical guidelines and requirements for pharmaceutical product registration and the maintenance of such registrations; * To maintain a forum for a constructive dialogue on scientific issues between regulatory authorities and the pharmaceutical industry on the harmonisation of the technical requirements for pharmaceutical products; * To contribute to the protection of public health in the interest of patients from an international perspective; * To monitor and update harmonised technical requirements leading to a greater mutual acceptance of research and development data; * To avoid spanergent future requirements through harmonisation of selected topics needed as a result of therapeutic advances and the development of new technologies for the production of medicinal products; * To facilitate the adoption of new or improved technical research and development approaches which update or replace current practices; * To encourage the adequate implementation and integration of common standards through the dissemination of, the communication of information about and coordination of training on, harmonised guidelines and their use; * And to develop policy for the ICH Medical Dictionary for Regulatory Activities Terminology (MedDRA) whilst ensuring the scientific and technical maintenance, development and dissemination of MedDRA as a standardised dictionary which facilitates the sharing of regulatory information internationally for medicinal products used by humans.". Since there have been only a few results, also nearby values are displayed.

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ICH Guidelines + (ICH’s mission has been embodied in its Art … ICH’s mission has been embodied in its Articles of Association as follows:* To make recommendations towards achieving greater harmonisation in the interpretation and application of technical guidelines and requirements for pharmaceutical product registration and the maintenance of such registrations;* To maintain a forum for a constructive dialogue on scientific issues between regulatory authorities and the pharmaceutical industry on the harmonisation of the technical requirements for pharmaceutical products;* To contribute to the protection of public health in the interest of patients from an international perspective;* To monitor and update harmonised technical requirements leading to a greater mutual acceptance of research and development data;* To avoid divergent future requirements through harmonisation of selected topics needed as a result of therapeutic advances and the development of new technologies for the production of medicinal products;* To facilitate the adoption of new or improved technical research and development approaches which update or replace current practices;* To encourage the adequate implementation and integration of common standards through the dissemination of, the communication of information about and coordination of training on, harmonised guidelines and their use;* And to develop policy for the ICH Medical Dictionary for Regulatory Activities Terminology (MedDRA) whilst ensuring the scientific and technical maintenance, development and dissemination of MedDRA as a standardised dictionary which facilitates the sharing of regulatory information internationally for medicinal products used by humans.lly for medicinal products used by humans.)

ICH Guidelines +