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 Center for Health Statistics
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