MDH Institutional Review Board
- Home: MDH IRB
- When Does a Study Require IRB Approval?
- Types of Review
- How to Submit a Study for Review
- Forms and Applications
- FAQ: Frequently Asked Questions
- Training, Tips, and Related Info
- Plain Language in your IRB Communications
- About the MDH IRB
- Membership and Requirements
- Contact Us
- Return to the Public Health Strategy and Partnership Division
Contact Info
MDH Institutional Review Board
Training, Tips, and Related Information
Institutional Review Board at the Minnesota Department of Health
Informed consent
- Informed Consent Tips, US Dept. of Health & Human Services
- Informed Consent Checklist, US Dept. of Health & Human Services
- Informed Consent of Subjects Who Do Not Speak English, US Dept. of Health & Human Services
- Related: Using Plain Language in your IRB Communications
Human Subjects Protections Training
- Protecting Human Research Participants Online Training and Certification
- Office for Human Research Protections’ (OHRP) Human Research Protection Foundational Training, US Dept. of Health & Human Services
- Centers for Disease Control and Prevention (CDC)
- Office of Human Research Protections (OHRP), US Dept. of Health & Human Services
Other related information
- The Belmont report: Ethical principles and guidelines for the protection of human subjects of research, US Dept. of Health & Human Services
- 45 CFR 46 (public welfare, protection of human subjects), US Dept. of Health & Human Services
- Distinguishing public health research and public health nonresearch (PDF), Centers for Disease Control and Prevention
- Human subject regulations decision charts, US Dept. of Health & Human Services
- Minn. Stat. § 13.04. Rights of subjects of data (Tennessen warning), Minnesota Office of the Revisor of Statutes
- The Minnesota Government Data Practices Act, Minnesota Dept. of Health
- Relevant provisions of the Minnesota Data Practices Act (PDF), Minnesota Dept. of Health
Last Updated: 01/31/2024