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Titlebook: Quick Guide to Good Clinical Practice; How to Meet Internat Cemal Cingi,Nuray Bayar Muluk Book 2017 Springer International Publishing Switz

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楼主: 审美家
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The Definition of GCP,ut the safety and efficacy of specific products and treatments has come from randomised, controlled clinical trials that are designed to answer important scientific and healthcare questions. Randomised controlled trials form the foundation for ‘evidence-based medicine’, but such research can be reli
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Preparation of Informed Consent, and to the ethical principles that have their origin in the Declaration of Helsinki. Before the beginning of the trial, the investigator should have the IRB/IEC’s written approval/favourable opinion of the written ICF and any other written information that is to be provided to subjects’.
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Preparation of Findings Tables,lso reduce the length of the manuscript and enhance readers’ understanding of the study results. However, while well-presented tables and figures in research papers can efficiently capture and present information, poorly crafted tables and figures can confuse readers and impair the effectiveness of
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Setting the Ideal Statistical Methods,r. Otherwise, the consequences of a poorly developed statistical approach may result in a failure to obtain extramural funding and result in a flawed clinical study that cannot adequately test the desired hypotheses. Statisticians provide design advice and develop the statistical methods that best c
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Setting the Size,en a well-conducted study may fail to answer its research question or to detect important effects or associations or may estimate those effects or associations too imprecisely. Similarly, if the sample size is too large, the study will be more difficult and costly, and the size may even lead to a lo
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