By On Oct 31, 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.
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.
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.
63 out of 100 based on 456 user ratings
199 Facebook Shares
102 Twitter tweet
268 Pinterest Pins
123 Google+ Shares
116 Thumblr Shares
51 Linkdkn Shares
© 2011 - 2018 Fietsen-winkel.info. All rights reserved.