By On Oct 07, 2018 Form Template
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.
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.
Form template types have almost no inherent semantic meaning, but aid solely as a means of organization for the designer/user. One notable exception: article type forms are the only ones listed in the Override form dropdown on the Write panel.
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