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WHO informed consent templates

Please 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 size

A 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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The UK's clinical trial toolkit

A 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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Some helpful tools to support community engagement

This tool box is focussed on HIV research, however some of the material could be adapted for other disease areas and these do provide good examples. Others views would be welcome - and other similar examples, perhaps for other disease areas?

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Brazil's Oswaldo Cruz Foundation, the largest Latin American biomedical research institution

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