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)

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Responsibilities of Directors of Research Studies Involving Human Subjects

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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

 

 

General Information

Office for Human Research Protections (OHRP) Guidance on Certificates of Confidentiality

 

National Institutes of Health (NIH) Certificates of Confidentiality Kiosk

 

OHRP Guidance on Withdrawal of Subjects from Research: Data Retention and Other Related Issues

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Research Involving Individuals with Questionable Capacity to Consent: Points to Consider (NIH)

 

OHRP Guidance on Research Involving Coded Private Information or Biological Specimens

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OHRP International Compilation of Human Subject Research Protections

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Ethical Issues in Research Involving Human Subjects: Bibliography (National Library of Medicine)

 

Timeline of Laws Related to the Protection of Human Subjects (National Institutes of Health)

 

Oral History Association Guidelines

 

Ethical Issues in Qualitative Research on Internet Communities (British Medical Journal Article)

 

American Psychological Association (APA) Board of Scientific Affairs Advisory Group on Conducting Research on the Internet Report

 

Ethical Issues in Reproductive Health Research (WHO)

 

American Geriatrics Society Position Statement on Research Involving the Elderly

 

American Geriatrics Society Position Statement on Informed Consent for Research Involving Human Subjects with Dementia

 

Bioethics Resources on the Web (National Institutes of Health)

 

American Statistical Association's Privacy and Confidentiality Website

 

University of Michigan's International Human Subjects Research Risks Compendium

 

World Health Organization Standards and Operational Guidance for Ethics Review of Health-Related Research with Human Participants