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Michigan Tech Institutional Review Board (Michigan TEch-IRB) for Human Subject Research

Michigan Technological University is committed to the protection of human subjects in research. To ensure that all investigators and research personnel receive a well-rounded education in human subjects protection, MTU has posted several important sources of information at this IRB website. To meet the standard of excellence set forward by Michigan Technological University, every MTU investigator is encouraged to give assurance that he/she has read the following required human subject protection documents.

Belmont Report: The Office of Human Research Protections (OHRP) considers it unethical for anyone involved in human subject research not to have read the Belmont Report. It describes and explains the ethical principles that should be followed by such investigators: respect for persons, beneficence and justice.

Code of Federal Regulations: All human subject researchers must read 45 CFR 46. This document is the Federal regulation that describes the authority and responsibility of Institutional Review Boards (IRBs) in protecting human subjects.

Michigan Tech Training Requirements for Human Subject Research DHHS Training Requirement: The Department of Health and Human Services (DHHS) has mandated that researchers receive training in human subject protections and the ethical conduct of research. Beginning October 1, 2000, any DHHS grant application must be accompanied by a cover letter indicating that training in human subject protections has been completed.

The training requirement set forth by DHHS can be met through participation in a computer based training program (CBT) or tutorial.

REGARDLESS of funding agency, you are required to undertake the on-line training session found at Human Subjects (CITI) Training
and obtain a certificate of completion. Investigators should maintain a file with copies of all relevant training.

Previous training will be accepted from the sites listed below. If you completed this training three or more years ago, you will need to complete the CITI Training. Please follow the link above.

Human Participant Protections Education for Research Teams (NIH)

Office for Human Research Protection (DHHS)

NOTE: Please allow a minimum of 2 weeks for IRB review and approval. The actual timeline may vary depending on the IRB meeting schedule. Please call if you have any questions.

RESOURCES

APPLICATIONS

INFORMED CONSENT

Templates and Sample Consent Forms

Tips on Informed Consent

Informed Consent Checklist

Informed Consent for non-english speakers

Exculpatory Languange in Informed Consent Documents



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