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ICH GCP

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International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. A standard for the design conduct performance monitoring auditing recording analyses and reporting of clinical trials that provides assurance that the data and reportedresults are credible and accurate and that the rights integrity and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing conducting recording and reporting trials that involve participation of human subjects to ensure that the RIGHTS SAFETY and WELLBEING of the trial subjects are protected. Ensure the CREDIBILITY of clinical trial data. ICH GCP E6 TABLE OF CONTENTS... read more


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ICH GCP
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International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. A standard for the design conduct performance monitoring auditing recording analyses and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate and that the rights integrity and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing conducting recording and reporting trials that involve participation of human subjects to ensure that the RIGHTS SAFETY and WELLBEING of the trial subjects are protected. Ensure the CREDIBILITY of clinical trial data. ICH GCP E6 TABLE OF CONTENTS
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