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ICH Guidelines are adopted by regulatory authorities and published on the ICH website. ICH also produces a standardised reference tool for medical terminology (MedDRA) in 27 languages and electronic standards for the transfer of regulatory information (ESTRI).
This International Conference on Harmonization (ICH) guidance addresses the choice of control group in clinical trials, discussing five principal types of controls, two important purposes of ...
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) brings together the medicines regulatory authorities and pharmaceutical industry around the world.
The ICH secretariat is responsible for day-to-day management of ICH, coordinating ICH activities as well as providing support to the assembly, the MC and working groups.
Through working groups of regulatory and industry experts, ICH produces harmonised technical requirements to ensure the development and registration of safe, effective, and high-quality medicines.