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Definitions from the WebIch Guidelines Clinical ResearchDefinition: The ICH Guidelines for Clinical Research are a set of internationally recognized standards and recommendations for conducting clinical trials, ensuring the safety, efficacy, and quality of new drugs or medical treatments. Sense 1 - Noun: Referring to a set of guidelines established by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), providing a framework for the conduct, design, and reporting of clinical trials. Example sentence: The compliance with ICH guidelines in clinical research is essential for ensuring the reliability and validity of study results. Sense 2 - Noun: Describing a collection of recommended practices and procedures for clinical research, aiming to harmonize global standards, facilitate the acceptance of data internationally, and expedite the drug development and approval process. Example sentence: By adhering to the ICH guidelines for clinical research, researchers can streamline the regulatory approval process for new drugs. Related Products: | ||||
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