- ICH Official web site : ICH
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals and develop ICH guidelines
- ICH Guidance Documents | FDA
This International Conference on Harmonization (ICH) guidance provides a unified standard for the European Union, Japan, and the United States to facilitate the mutual acceptance of clinical data
- ICH Official web site : ICH
ICH has produced a comprehensive set of safety Guidelines to uncover potential risks like carcinogenicity, genotoxicity and reprotoxicity A recent breakthrough has been a non-clinical testing strategy for assessing the QT interval prolongation liability: the single most important cause of drug withdrawals in recent years
- Welcome to the ICH Official Website | ICH
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals and develop ICH guidelines
- International Council for Harmonisation of Technical Requirements for . . .
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is an initiative that brings together regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of pharmaceutical product development and registration
- The International Council for Harmonisation (ICH) - IFPMA
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is a unique platform bringing together regulatory authorities (RAs) and pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals, as well as establishing common standards and guidelines
- ICH | European Medicines Agency (EMA)
The International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) brings together regulatory authorities and the pharmaceutical industry
- From guideline to practice: three years of ICH S11 insights and . . .
The ICH S11 guideline was the first to require a standardised weight of evidence (WoE) approach to guide the nonclinical development strategy and determine the need for additional (juvenile) non-clinical studies
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