Depending on your role here at U-M, there are several required trainings that are related to human subjects research. This is a set of the most commonly required training.
The Program for Education and Evaluation in Responsible Research and Scholarship (PEERRS)
PEERRS certification may be required for participation on a study or project team, depending on your role (e.g., Principal Investigator), the funding source (e.g., NSF), and/or the type of research (e.g., human subjects).
The Health Insurance Portability and Accountability Act privacy rule governs both clinical and human subjects research areas. Training is required for anyone who has access to identifiable patient data.
Collaborative Institutional Training Initiative (CITI) Program - Good Clinical Practice Course
The CITI Program’s GCP for Clinical Trials with Investigational Drugs and Medical Devices - U.S. FDA course is designed specifically for clinical researchers participating in human subjects research to have an understanding and knowledge of the federal regulations, International Conference for Harmonisation (ICH) Regulations, and Good Clinical Practice guidelines that apply to clinical research. PDF - Instructions for Accessing GCP Modules (CITI Program)
Social Behavioral Research Best Practices Course
The goal of this e-learning course is to enable learners to apply good clinical practice (GCP) principles to clinical research investigations involving human subjects as they specifically apply to social and behavioral research.
If you have questions about any of the resources on this page, please contact the sponsoring office directly. MICHR is not responsible for the content of these resources.
Resources on this page may not be an exhaustive list. If you know of other resources in this category, please let us know using the "Suggest a Resource" link at the bottom of the page.