[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"detail-sidebar-cat-1-en-105":3,"doc-seo-281039-105":53,"doc-detail-281039-en":127},{"code":4,"msg":5,"data":6},0,"success",[7,14,19,24,29,34,39,44,49],{"id":8,"doc_module":9,"doc_module_name":10,"category_name":11,"show_sort_weight":12,"slug":13},11,1,"Template","Presentations",90,"presentations",{"id":15,"doc_module":9,"doc_module_name":10,"category_name":16,"show_sort_weight":17,"slug":18},12,"Resumes",80,"resumes",{"id":20,"doc_module":9,"doc_module_name":10,"category_name":21,"show_sort_weight":22,"slug":23},14,"Invoices",70,"invoices",{"id":25,"doc_module":9,"doc_module_name":10,"category_name":26,"show_sort_weight":27,"slug":28},15,"Posters",60,"posters",{"id":30,"doc_module":9,"doc_module_name":10,"category_name":31,"show_sort_weight":32,"slug":33},16,"Social Media",50,"social-media",{"id":35,"doc_module":9,"doc_module_name":10,"category_name":36,"show_sort_weight":37,"slug":38},17,"Forms",40,"forms",{"id":40,"doc_module":9,"doc_module_name":10,"category_name":41,"show_sort_weight":42,"slug":43},18,"Letters",30,"letters",{"id":45,"doc_module":9,"doc_module_name":10,"category_name":46,"show_sort_weight":47,"slug":48},21,"Paper Templates",5,"papers-templates",{"id":50,"doc_module":9,"doc_module_name":10,"category_name":51,"show_sort_weight":4,"slug":52},158,"General","general-158",{"code":4,"msg":54,"data":55},"ok",{"site_id":56,"language":57,"slug":58,"title":59,"keywords":60,"description":61,"schema_data":62,"social_meta":120,"head_meta":122,"extra_data":124,"updated_unix":126},105,"en","texas-am-international-university-irb-criteria-protocol-for-human-subjects-in-research","Texas A&M International University IRB - Criteria: Protocol for Human Subjects in Research","","Texas A&M International University Institutional Review Board (IRB) criteria outline the protocol requirements for research involving human subjects. The document provides a checklist for submitting Forms I and II, including expedited review criteria and a structured summary cover sheet. It collects detailed information on investigators, risk level, subject demographics, invasive or sensitive procedures, confidentiality or anonymity provisions, and retention and destruction of coded replies. It also presents the request for expedited review and the required sections for selection of subjects, procedures, risks and benefits, and signatures for IRB consideration.",{"@graph":63,"@context":119},[64,80,102],{"@type":65,"itemListElement":66},"BreadcrumbList",[67,71,74,77],{"item":68,"name":69,"@type":70,"position":9},"https://docshare.wps.com","Home","ListItem",{"item":72,"name":10,"@type":70,"position":73},"https://docshare.wps.com/template/",2,{"item":75,"name":36,"@type":70,"position":76},"https://docshare.wps.com/template/forms/",3,{"item":78,"name":59,"@type":70,"position":79},"https://docshare.wps.com/template/texas-am-international-university-irb-criteria-protocol-for-human-subjects-in-research/281039/",4,{"url":78,"name":59,"@type":81,"image":82,"author":87,"headline":59,"publisher":90,"fileFormat":93,"inLanguage":57,"description":61,"dateModified":94,"datePublished":95,"encodingFormat":93,"isAccessibleForFree":96,"interactionStatistic":97},"DigitalDocument",{"url":83,"@type":84,"width":85,"height":86},"https://docshare.wps.com/thumbnails/texas-am-international-university-irb-criteria-protocol-for-human-subjects-in-research/281039.png","ImageObject",442,249,{"name":88,"@type":89},"Aran","Person",{"url":68,"name":91,"@type":92},"DocShare","Organization","application/pdf","2026-11-03","2026-09-16",true,{"@type":98,"interactionType":99,"userInteractionCount":101},"InteractionCounter",{"@type":100},"ViewAction",7,{"@type":103,"mainEntity":104},"FAQPage",[105,111,115],{"name":106,"@type":107,"acceptedAnswer":108},"What information is required in Form I summary cover sheet?","Question",{"text":109,"@type":110},"Form I requests investigator details, project title, an estimate of risk to subjects, gender distribution, whether procedures are invasive/sensitive, sensitive subject matter types, confidentiality/anonymity provisions, and retention and secure storage or destruction options.","Answer",{"name":112,"@type":107,"acceptedAnswer":113},"Which types of research qualify for expedited review under the IRB criteria?",{"text":114,"@type":110},"Expedited review may apply when human-subject involvement fits specified categories, including normal educational practices, certain educational tests and survey/interview/observation activities with confidentiality safeguards, publicly available existing data or records, department/agency head-approved program evaluation studies, and certain taste and food quality evaluation studies under defined conditions.",{"name":116,"@type":107,"acceptedAnswer":117},"What sections must be completed in Form II for IRB consideration?",{"text":118,"@type":110},"Form II includes project title and principal investigator information with an affidavit referencing the Belmont Report, plus detailed sections for selection and sources of subjects, experimental procedures, risks and benefits (including alternatives and ability to withdraw), and required signatures and dates for IRB use.","https://schema.org",{"og:url":78,"og:type":121,"og:title":59,"og:site_name":91,"og:description":61},"article",{"robots":123,"canonical":78},"index,follow",{"doc_id":125,"site_id":56},281039,1791562909,{"code":4,"msg":5,"data":128},{"doc_id":125,"user_id":129,"nickname":88,"user_avatar":130,"doc_module":9,"category_id":35,"category_name":36,"doc_title":59,"doc_description":61,"doc_content":131,"file_id":132,"file_url":133,"file_type":134,"file_size":135,"view_count":101,"is_deleted":4,"is_public":9,"is_downloadable":9,"audit_status":9,"page_count":8,"language":136,"language_code":57,"site_id":56,"html_lang":57,"table_of_contents":137,"faqs":138,"seo_title":139,"seo_description":61,"update_tm":140,"read_time":79},137455076865,"https://ap-avatar.wpscdn.com/davatar_29158cc5080c5b710cf443261637dec0","Texas A&M International University IRB  \nCriteria: Protocol for Human Subjects in Research  \n􀀀 Forms I & II are to be typed  \n􀀀 Check list are to be filled-out & submitted  \n􀀀 Consent form(s) and instrument(s) to be submitted  \nPlease check off or provide details on the following (enter N/A if not applicable) . 􀀀 Expedited Review  \nSee Page 2  \nForm I Summary Cover Sheet  \nPrinciple Investigator Name:   􀀀 Faculty 􀀀 Graduate Student* College Dept.  E-mail   Phone  Project Title    \n___________________________________________________________  \nSubjective Estimate of Risk to Subject: 􀀀 None 􀀀 Low 􀀀 Moderate 􀀀 High  \nGender of Subjects: 􀀀 Male 􀀀 Female  \nInvasive/ Sensitive Procedure: 􀀀 Yes 􀀀 No Sensitive Subject Matter: 􀀀 Yes 􀀀 No  \n􀀀 Blood samples  \n􀀀 Physical measurements 􀀀 Psychological Inventory  \n􀀀 DNA  \n􀀀 Urine samples  \n􀀀 Stress Exercise  \n􀀀 Review of Medical Records  \n􀀀 Other (specify)    \n􀀀 Alcohol, Drugs, Sex  \n􀀀 Depression/Suicide  \n􀀀 Learning Disability 􀀀 Other (specify)   \nUse of 􀀀 Video or 􀀀 Audio Tapes (please indicate) Provisions for Confidentiality/Anonymity  \nRetained 􀀀 Yes 􀀀 No 􀀀 Replies Coded  \nLength of time retained   􀀀 Secure Storage  \nDestroy/Erase 􀀀 Yes 􀀀 No 􀀀 Anonymous Response  \nOther (explain)   􀀀 Confidential Response  \nUse specified in consent form? 􀀀 Yes 􀀀 No Use/Access to tapes:    \n* Must include signature of committee chair on protocol  \nREQUEST FOR EXPEDITED REVIEW:  \nUnless otherwise required by department or agency heads, research activities in which the only involvement of human subjects will be in one or more of the following categories qualify for expedited review by the IRB. Please check the box that indicates which criterion you believe applies to your research:  \n􀀀 Research conducted in established or commonly accepted educational settings, involving normal educational practices, such as:  \n♦ research on regular and special education instructional strategies, or  \n♦ research on the effectiveness of or the comparison among instructional techniques, curricula, or classroom management methods.  \n􀀀 Research involving the use of educational tests (cognitive, diagnostic, aptitude, achievement), survey procedures, interview procedures or observation of public behavior, unless:  \n♦ information obtained is recorded in such a manner that human subjects can be identified, directly or through identifiers linked to the subjects; and  \n♦ any disclosure of the human subjects’ responses outside the research could reasonably place the subjects at risk of criminal or civil liability or be damaging to the subjects’ financial standing, employability, or reputation.  \n􀀀 Research involving the use of educational tests (cognitive, diagnostic, aptitude, and achievement), survey procedures, interview procedures, or observation of public behavior that is not except under the second bullet of this section, if:  \n♦ the human subjects are elected or appointed public officials or candidates for public office, or  \n♦ federal statute(s) require(s) without exception that the confidentiality of the personally identifiable information will be maintained throughout the research and thereafter.  \n􀀀 Research involving the collection or study of existing data, documents, records, pathological specimens, or diagnostic specimens, if these sources are publicly available or if the information is recorded by the investigator in such a manner that subject cannot be identified, directly or through identifiers linked to the subjects.  \n􀀀 Research and demonstration projects that are conducted by or subject to the approval of department or agency heads, and that are designed to study, evaluate, or otherwise examine:  \n♦ public benefit or service programs;  \n♦ procedures for obtaining benefits or services under these programs;  \n♦ possible changes in or alternatives to those programs or procedures; or  \n♦ possible changes in methods or levels of payment for benefits or services under those programs.  \n􀀀 Taste and food quality evaluation","cbCais6ymaFJvfm8","https://ap.wps.com/l/cbCais6ymaFJvfm8","pdf",823436,"English","# Form I Summary Cover Sheet\n## Expedited Review Criteria\n# Request for Expedited Review\n## Form II - Project and Consent Information\n## Selection of Subjects\n## Description of Experimental Procedure\n## Risks and Benefits to Subjects\n## Signatures and IRB Use","[{\"question\":\"What information is required in Form I summary cover sheet?\",\"answer\":\"Form I requests investigator details, project title, an estimate of risk to subjects, gender distribution, whether procedures are invasive/sensitive, sensitive subject matter types, confidentiality/anonymity provisions, and retention and secure storage or destruction options.\"},{\"question\":\"Which types of research qualify for expedited review under the IRB criteria?\",\"answer\":\"Expedited review may apply when human-subject involvement fits specified categories, including normal educational practices, certain educational tests and survey/interview/observation activities with confidentiality safeguards, publicly available existing data or records, department/agency head-approved program evaluation studies, and certain taste and food quality evaluation studies under defined conditions.\"},{\"question\":\"What sections must be completed in Form II for IRB consideration?\",\"answer\":\"Form II includes project title and principal investigator information with an affidavit referencing the Belmont Report, plus detailed sections for selection and sources of subjects, experimental procedures, risks and benefits (including alternatives and ability to withdraw), and required signatures and dates for IRB use.\"}]","Texas A&M International University IRB - Criteria: Protocol for Human Subjects in Research | PDF",1789563749]