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.
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.
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.
68 out of 100 based on 906 user ratings
394 Facebook Shares
202 Twitter tweet
532 Pinterest Pins
244 Google+ Shares
232 Thumblr Shares
101 Linkdkn Shares
© 2011 - 2019 Fietsen-winkel.info. All rights reserved.