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E6 refers to the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline on Good Clinical Practice (GCP). This guideline sets out the standards for designing, conducting, recording, and reporting clinical trials involving human subjects. It ensures that the rights, safety, and well-being of trial participants are protected, and that the data generated is reliable and credible.

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Q: What does E6 stand E6 in ICH GCP guidelines?
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