By On Oct 02, 2018 Form Template
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.
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.
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.
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