By On Oct 25, 2018 Form Template
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.
Throughout this series I will cover CDASH 1.1 best practice recommendations for specific domains, provide examples from my own experience, and discuss common questions that arise during eCRF development. The intent of these articles is to provide concrete examples for those learning and implementing CDASH eCRFs, and a forum for others to share their own experiences and best practice recommendations.
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.
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