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A tool for training and promoting Quality Practices in Basic Biomedical Research (QPBR) concepts inA TDR publication for promoting quality practices in research
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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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Support for health systems researchPractihc (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.
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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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