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The International Council on Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is a global scientific and regulatory organisation that develops and maintains guidelines for the pharmaceutical industry. These guidelines are adopted by regulatory authorities in many countries around the world, and they aim to ensure that medicines are safe, effective, and of high quality.

The ICH was founded in 1990 by the European Union, Japan, and the United States. Since then, it has expanded to include 16 member countries and regions and three observer organisations. The ICH's work is carried out by five expert committees, which cover the following areas: quality, safety, efficacy, and regulatory affairs.

The ICH's guidelines are developed through a consensus-based process involving experts from industry, academia, and regulatory authorities. The guidelines are then published on the ICH's website and are made available to the public. The ICH also provides training and support to help industry and regulatory authorities implement the guidelines.

The ICH's work has had a significant impact on the global pharmaceutical industry. The guidelines have helped to ensure that medicines are safe, effective, and of high quality. They have also helped to reduce the cost of drug development and to speed up the time it takes to bring new medicines to market.

The ICH is a vital organisation that plays a key role in the global pharmaceutical industry. The guidelines developed by the ICH help to ensure that medicines are safe, effective, and of high quality. The ICH also provides training and support to help industry and regulatory authorities implement the guidelines.

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