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GLADE PRESENTATION OF RESEARCH PROJECTS (FINAL) STANDARD OPERATING PROCEDURES (SOP) Version 5.0 (May 10, 2024)This document aims to standardize the presentation format of research projects by investigators
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Review the SOP template provided by the organization
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Fill in all relevant information such as title, date, and version number
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Include the purpose, scope, responsibilities, and procedures in the SOP
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Provide a detailed description of each step in the clinical research process
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Who needs clinical research sops?

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Clinical researchers
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Clinical research coordinators
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Clinical research sponsors
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Regulatory authorities
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Clinical research SOPs (Standard Operating Procedures) are established instructions designed to help researchers conduct clinical trials in an organized and consistent manner.
Researchers, clinical trial sponsors, and other individuals involved in conducting clinical research are required to follow and file clinical research SOPs.
Clinical research SOPs are typically filled out by following the specified guidelines and templates provided by regulatory authorities or the institution conducting the research.
The purpose of clinical research SOPs is to ensure that clinical trials are conducted ethically, safely, and in compliance with regulations and guidelines.
Clinical research SOPs must include details on study protocols, participant recruitment, data collection methods, adverse event reporting, and other critical aspects of the clinical trial.
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