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hello there and welcome today well be talking about one of the most important components in clinical research and for patients in general informed consent what is it lets find out what everybody really everybody should know the information and consent process must be documented in a logical and chronologically comprehensible way its particularly important that the informed consent form is never filled with the date in advance the patients or the legal representatives must always enter the current date by themselves otherwise nobody can see if the patient really consented prior to the study start or after lets talk about the content of the information obtained from every subject the large size of this document is partly attributable to the fact that certain information is required by gcp as well as by national legislation respectively the informed consent must contain a note that the clinical study is part of a research project and the purpose of the study and the name of the spons