IRB Application Resources
Click here to access UNH Institutional Review Board for the Protection of Human Subjects in Research (IRB) application materials, including sample consent form templates.
Studies submitted to the IRB for review must comprise a completed application form, including appropriate signatures, a research protocol (narrative), documentation of completion of the UNH Web-based training on human subjects protections*, and any required supporting materials. IMPORTANT! If the researcher is a student, the faculty advisor must sign the application form and attach a letter of support for the research stating the student’s experience and the level of supervision to be provided.
*Effective September 1, 2011, applications to the UNH IRB must include for the project director (applicant) documentation of completion of the UNH Web-based training on human subjects protections. The UNH IRB will not review applications missing this documentation. See http://unh.edu/research/irb-training for more information.
Completed applications need to be submitted to Research Integrity Services, via email (to Julie Simpson or Kathleen Stilwell), fax (603-862-3564), in-person, or by campus/US mail (Service Building, 51 College Road, Durham, NH 03824-3585).
Faculty, staff, and students who would like assistance in developing research protocols, or would like to discuss any issues related to their research studies, should contact Julie Simpson, Director of Research Integrity Services (RIS). Dr. Simpson is also available to talk to classes or groups of faculty, staff, or students about protecting human subjects in research and the IRB.
UNH IRB Resource Materials | |
IRB Guide for Researchers (updated February 2013) | |
Activities Involving Human Subjects and IRB Approval (updated January 2013) | |
Responsibilities of Directors of Research Studies Involving Human Subjects | |
Guidelines for Writing a Research Protocol to Submit to the IRB | |
Information Individuals in New Hampshire are Legally Required to Report | |
Informed Consent Format and Checklist | |
Tips for Writing Easy-to-Read Informed Consent Documents | |
Child Assent Guidelines | |
Confidentiality Guidelines | |
Guidelines for Involving in Research Institutionalized and Special Populations in Health Care Related Setting | |
Guidelines for Conducting Web-Based Survey Research | |
Documents | |
UNH Federalwide Assurance for the Protection of Human Subjects | |
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