This blog is closed to new posts due to inactivity. The post remains here as part of the network’s archive ...
This blog is closed to new posts due to inactivity. The post remains here as part of the network’s archive ...
Today we have launched the pilot for the Global Health Clinical Trials website. We aim for this to be a ...
Thiscourse covers the essentials of study design and protocol development, bioethics,good clinical practice (GCP), data management, regulatory affairs, safety monitoring,and practical management skills.
Transparency in the conduct and reporting of clinical trials is supported by the guidance produced on the content of clinical trial protocols and reporting standards for clinical trials. While the principle features of the statistical analysis are required within this guidance it is generally accepted that a separate Statistical Analysis Plan is also developed as the level of detail appropriate for a SAP is excessive for a protocol. However, there is no detailed guidance on the content of a SAP and consequently, there is marked variation in practice.
Secondary analysis of clinical trial data reveals dengue burden
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