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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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Support for health systems research

Practihc (Pragmatic Randomized Controlled Trials in HealthCare) is a European Union-funded converted action which provides open-access tools, training and mentoring to researchers in developing countries who are interested in designing and conducting pragmatic randomized controlled trials of healthcare interventions.
Practihc is a collaboration of leading trialists from eleven countries who aim to improve health systems by increasing capacity to evaluate healthcare delivery systems, health policy, public health and clinical choices an identify those optoins which are most effective.

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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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US trial support, resources and tools

These are aimed at US based trials but there are some globally applicable resources and content.

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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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Bookmarked by The Editorial Team on 13 Jul 2010
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