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  • 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 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
  • ICH Official web site : ICH
    The Q3C ICH Guideline was finalised under Step 4 in July 1997, providing recommendations on the use of less toxic solvents in the manufacture of drug substances and dosage forms, and setting pharmaceutical limits for residual solvents (organic volatile impurities) in drug products Maintenance Process
  • ICH Official web site : ICH
    Those are the cross-cutting topics which do not fit uniquely into one of the Quality, Safety and Efficacy categories It includes the ICH medical terminology (MedDRA), the Common Technical Document (CTD) and the development of Electronic Standards for the Transfer of Regulatory Information (ESTRI)
  • ICH HARMONISED GUIDELINE GUIDELINE FOR GOOD CLINICAL PRACTICE E6(R3)
    The objective of this ICH GCP Guideline is to provide a unified standard to facilitate the mutual acceptance of clinical trial data for ICH member countries and regions by applicable regulatory authorities This guideline builds on key concepts outlined in ICH E8(R1) General Considerations for Clinical Studies
  • ICH Official web site : ICH
    The work carried out by ICH under the Efficacy heading is concerned with the design, conduct, safety and reporting of clinical trials It also covers novel types of medicines derived from biotechnological processes and the use of pharmacogenetics pharmacogenomics techniques to produce better targeted medicines
  • ICH Official web site : ICH
    The Assembly of the International Council for Harmonisation (ICH) met in-person on 13 14 May 2025, in Madrid, Spain in parallel of meetings of 11 Working Groups, and preceded by meetings of the ICH Management Committee (MC) and the MedDRA Steering Committee
  • ICH Official web site : ICH
    You can explore in the below table the index of all ICH Guidelines, finalised or under development, on the topics of Quality, Safety, Efficacy and Multidisciplinary Please select first the relevant topic You can then search by ICH Step status, date, and or by keyword You can also download the information in a spreadsheet by clicking on




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