The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is a unique global initiative that brings together regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of drug registration. Its mission is to promote public health by achieving greater harmonisation in the interpretation and application of technical guidelines and requirements for pharmaceutical product registration, thereby reducing duplication of testing and reporting carried out during the research and development of new medicines.
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ICH develops guidelines that are recognized as the international standard for the development, registration, and post-approval of pharmaceutical products.
Facilitates collaboration between regulatory authorities and the pharmaceutical industry across the globe to ensure the safety, efficacy, and quality of medicines.
Offers training sessions and workshops to disseminate knowledge on ICH guidelines and their implementation.
Aims to achieve regulatory convergence to reduce duplication of efforts in the development and review of new medicines.
Focuses on improving public health by ensuring that safe, effective, and high-quality medicines are developed and registered efficiently.
ICH members include regulatory bodies from the EU, USA, Japan, Canada, Switzerland, and representatives from the pharmaceutical industry.
ICH guidelines cover a wide range of topics, including quality, safety, efficacy, and multidisciplinary guidelines.
ICH guidelines have significantly influenced the regulatory processes for pharmaceuticals worldwide, leading to more efficient drug development processes.
The guidelines and standards set by ICH are adopted by many countries beyond its membership, demonstrating its global influence.
ICH continuously reviews and updates its guidelines to reflect the latest scientific and technical advancements in pharmaceutical development.
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