Titlebook: Success in Academic Surgery: Clinical Trials; Timothy M. Pawlik,Julie A. Sosa Book 20141st edition Springer-Verlag London 2014 Clinical tr

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Small-Intestine

Clinical Trials: Ensuring Quality and Standardization,he start and conclusion to a trial, the principal investigator should refer to the Consolidated Standards of Reporting Trials checklist and flow diagram to provide accurate performance and documentation of the outcomes.

Incorporate

Regulatory Considerations in Human Subjects Research,ug Administration (FDA) regulations relating to such research. This chapter will review the historical context under which these regulations were developed, provide an overview of the current regulatory requirements that must be met to perform human subjects research, and offer some practical considerations for new academic investigators.

forebear

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DRAFT

Publishing a Clinical Trial,number of resources and checklists are available for ensuring all of the necessary components of the write-up are included in the manuscript. The trial results should be published, irrespective of the findings.

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Expertise

Clinical Trials: Ensuring Quality and Standardization,hese trials is of paramount importance to retain the confidence of the public in human subjects research. Prior to initiating a clinical trial, the surgical trialist is advised to familiarize themselves with the regulatory documents and processes within the Belmont Report, good clinical practice, an