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MRC Guidelines for Good Clinical Practice in Clinical Trials (1998)MRC guidance on GCP. Slightly ageing now (there is a revision in draft) but still a useful reference.
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Bookmarked by Andy Burke on 31 Aug 2010
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Latest TDR news * Call for investment in health information
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Bookmarked by The Editorial Team on 6 Aug 2010
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Science and Technology in Kenya, Does Kenya Care?The Grand Debate aimed to drive a discussion of Science and Technology (S&T) and its relevance to Kenyan development. With utube link to programmed debate
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Bookmarked by Roma Chilengi on 27 Jul 2010
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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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Bookmarked by The Editorial Team on 13 Jul 2010
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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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Bookmarked by The Editorial Team on 13 Jul 2010
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