By On Oct 19, 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.
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.
One of the features of ProForm is the ability to create a single template capable of rendering any form that is designed in the module. Creating a reusable form template is simple and it can provide the same consistent UI to all of your forms, reducing the amount of work it takes to create a new form.
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