The Medical IRB reviews all biomedical research involving human subjects (including VAMC and FDA-regulated research). IRB members include individuals with a broad range of expertise. The Medical IRB members are appointed by the director of the Office of Research Integrity.<\/p>\n
All research involving the use of human subjects subject to the Marshall University Human Research Protection Program MUST be submitted to an IRB designated by Marshall University for review and approval PRIOR to initiation of the project.<\/p>\n
Applications for medical\/biological research should be submitted to IRB #1. Applications for studies that have been approved by any Central IRB should be submitted to the MU CIRB (under IRB#1).<\/p>\n
All submission forms are available on the IRBNet website,<\/a>\u00a0the system that is used for all IRB submissions. The IRBNet User Manual is available here<\/a> and in the Quick Links on the right-hand sidebar.<\/p>\n Protocol Flow Chart<\/a> Meeting Dates\/Deadlines\u00a0– Meets second Wednesday of each month. Submission must be received 30 days prior to the meeting.\u00a0<\/strong><\/p>\n IRB#1 Member List<\/a>\u00a0<\/a> The Belmont Report<\/a> Health Insurance Portability and Accountability Act (HIPAA)<\/a> Guide For Determining When Protocols Involving Coded Private Information or Biological or <\/a>Specimens Meet the Federal Definition of \u201cHuman Research\u201d<\/a><\/p>\n \n","protected":false},"excerpt":{"rendered":" The Medical IRB reviews all biomedical research involving human subjects (including VAMC and FDA-regulated research). IRB members include individuals with a broad range of expertise. The Medical IRB members are appointed by the director of the Office of Research Integrity. All research involving the use of human subjects subject to the Marshall University Human Research<\/p>\n","protected":false},"author":15,"featured_media":0,"parent":777,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-353","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/pages\/353","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/users\/15"}],"replies":[{"embeddable":true,"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/comments?post=353"}],"version-history":[{"count":12,"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/pages\/353\/revisions"}],"predecessor-version":[{"id":3097,"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/pages\/353\/revisions\/3097"}],"up":[{"embeddable":true,"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/pages\/777"}],"wp:attachment":[{"href":"https:\/\/www.marshall.edu\/ori\/wp-json\/wp\/v2\/media?parent=353"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}Other Forms for Investigators<\/h2>\n
\nConflict of Interest Checklist (Researchers)<\/a>\u00a0(Word<\/a>,\u00a0PDF<\/a>)
\nExpedited Categories 1-9<\/a>
\nEmergency Use Letter Template<\/a><\/p>\nForms for IRB Members<\/h2>\n
\nEducation Requirements<\/a>
\nConflict of Interest Checklist (IRB Members)<\/a>\u00a0<\/span>(Word<\/a>,\u00a0<\/span>PDF<\/a>)
\n<\/span>IRB Guest Non-Disclosure Agreement<\/a><\/span><\/p>\nEthics Reports<\/h2>\n
\nDeclaration of Helsinki<\/a>
\nNuremberg Code (Directives for Human Experimentation)<\/a><\/p>\nRegulations<\/h2>\n
\nCode of Federal Regulations (45 CFR 46)<\/a><\/p>\nAdditional Guidance<\/h2>\n