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This article was downloaded by: [T&F Internal Users], [Laura Ronnie] On: 03 January 2012, At: 08:45 Publisher: Routledge Inform Ltd Registered in England and Wales Registered Number: 1072954 Registered
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A brief protocol is a document that outlines the key elements and procedures of a study or project, typically summarizing information necessary for compliance with regulatory standards.
Researchers or organizations conducting clinical trials, studies, or specific projects that require regulatory oversight are typically required to file a brief protocol.
To fill out a brief protocol, an individual should gather all relevant study information, complete the designated sections of the document with accurate data, and ensure compliance with organizational or regulatory guidelines.
The purpose of a brief protocol is to provide a concise summary of the research objectives, methodology, and compliance requirements to facilitate review and approval processes.
Information typically required includes study title, objectives, design, population details, intervention methods, endpoints, and data analysis plans.
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