By On Oct 02, 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.
Do not be concerned by the length of these templates. They are long only because they contain guidance and explanations which are for you and which you will not include in the informed consent forms that you develop and provide to participants in your research.
standard lettering is used for explanations to researchers only and must not be included in your consent forms. The explanation is provided in black, and examples are provided in red in italics. Suggested questions to elucidate understanding are given in black in italics.
42 out of 100 based on 154 user ratings
67 Facebook Shares
35 Twitter tweet
90 Pinterest Pins
41 Google+ Shares
39 Thumblr Shares
17 Linkdkn Shares
© 2011 - 2018 Fietsen-winkel.info. All rights reserved.