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.
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.
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.
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