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In this tutorial, the focus is on the critical concept of informed consent in clinical research. It emphasizes that the information and consent process must be documented logically and chronologically. Specifically, the informed consent form should not be predated; patients or their legal representatives must enter the current date themselves to ensure clarity on whether consent was given before or after the study began. The content of the informed consent document is extensive, complying with Good Clinical Practice (GCP) and national legislation requirements. It must clearly state that the clinical study is part of a research project, outlining the study's purpose and the sponsor's name.