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WHO informed consent templatesPlease note that these are templates developed by the WHO ERC to assist the Principal Investigator in the design of their informed consent forms (ICF). It is important that Principal Investigators adapt their own ICFs to the outline and requirements of their particular study. The logo of the Institution must be used on the ICF and not the WHO logo.
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A tool to help calculate sample sizeA free software package that can simulate Randomized Controlled Clinical Trials (RCTs). With the CTS a user can explore aspects of the design, conduction and analyses of RCTs
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US trial support, resources and toolsThese are aimed at US based trials but there are some globally applicable resources and content.
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The UK's clinical trial toolkitA very detailed website based around the EU clinical trial directive aimed at those running trials in the UK. Although many of the local references to the approval processes may not apply there are some good resources and examples on this site. Many of the scenarios and guidance as generic application.
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Lots of clinical trial templates, resources and examplesThis is an excellent website design really for US based researchers as and therefore has an NIH/FDA focus. However there are documents and examples that can be taken and ammended and they are generic for all trials and disease areas.
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