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I looked back you are going for a long presser you last his tool.[E3] If the study staff has been trained in the Singapore Guideline for Good Clinical Practice (SGGCP), do they need to be re-trained in the ICH E6 GCP after the port over of the clinical trials regulations?[E4] If there is a change of Principal Investigator (PI) for a clinical trial, how can this change be documented on the Signature Sheet?[H1] What are the basic principles of an informed consent process?[H2] What are the regulatory requirements for informed consent?

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