By On Oct 31, 2018 Form Template
These templates include examples of key questions that may be asked at the end of each section, that could ensure the understanding of the information being provided, especially if the research study is complex. These are just examples, and suggestions, and the investigators will have to modify the questions depending upon their study.
Once a new DF/HCC protocol has been created, it must be submitted to the Office for Human Research Studies before research can begin. Office for Human Research Studies has developed application forms that request study information. This information is used to determine what type of review the new submission will require.
Please note that these are templates developed by the WHO ERC to assist the Principal Investigator in the design of their informed consent forms. It is important that Principal Investigators adapt their own ICFs to the outline and requirements of their particular study.
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