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It includes guidance on general information, study title and protocol details, introduction and background, specific aims, methods and analysis, participant population, recruitment methods, payments, informed consent and consent process, privacy/confidentiality and data disposition, risks and potential benefits, and any clinical research or trial details. 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Using the guidance will help facilitate timely IRB review. Keep all sections A through J below. If a section is not applicable, you can note that in the section, but do not delete the section.\nGeneral Information (Optional)\nStudy Title:\nProtocol Number:\nPrincipal Investigator:\nIntroduction and Background\nSpecific Aims/Study Objectives\nMethods, Materials and Analysis\nResearch Population, Recruitment Methods and Payments/Compensation\nParticipant/Subject Population\nRecruitment Methods\nCompensation/Payments\nInformed Consent\nInformed Consent Process\nFacilitate Understanding\nDocumentation\nAdditional Considerations\nParticipant/Subject Privacy, Confidentiality and Data Disposition\nParticipant/Subject Privacy\nConfidentiality\nData Disposition\nPotential Research Risks or Discomforts to Participants\nPotential Benefits of the Research\nClinical Research and/or Clinical Trials\nInvestigator Qualifications, Roles and Training\nInvestigator Qualifications\nRoles and Research Duties\nTraining and Oversight\nTranslator (if applicable)","cbCainwTSIZobEcC","https://ap.wps.com/l/cbCainwTSIZobEcC","docx",23139,"English","# General Information (Optional)\n## Study Title\n## Protocol Number\n## Principal Investigator\n# Introduction and Background\n## Specific Aims/Study Objectives\n## Methods, Materials and Analysis\n# Research Population and Recruitment\n## Participant/Subject Population\n## Recruitment Methods\n## Compensation/Payments\n# Informed Consent\n## Informed Consent Process\n## Facilitate Understanding\n## Documentation\n# Additional Considerations\n## Participant/Subject Privacy, Confidentiality and Data Disposition\n## Participant/Subject Privacy\n## Confidentiality\n## Data Disposition\n## Potential Research Risks or Discomforts to Participants\n## Potential Benefits of the Research\n## Clinical Research and/or Clinical Trials\n## Investigator Qualifications, Roles and Training\n## Investigator Qualifications\n## Roles and Research Duties\n## Training and Oversight\n## Translator (if applicable)","[{\"question\":\"What participant-related topics are required besides recruitment?\",\"answer\":\"It includes participant/subject privacy, confidentiality, and data disposition, along with informed consent process, potential risks or discomforts, and potential benefits of the research.\"}]","Research Plan - Version 8 - complete sections A through J | DOCX",1788236582]