Our aim is to provide study teams with the tools and resources they need when facing their day-to-day challenges while conducting clinical and health research at the University of Michigan.
This self-guided course is designed to outline best practices for clinical research. While these best practices are based in the principles of Good Clinical Practice (GCP) from the International Conference on Harmonization, this course is not able to fulfill requirements to complete GCP training.
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.
To address the need for consistent training and assessment of research skills, MICHR has collaborated three other universities to create the DIAMOND portal. The portal is a digital collection that serves as a sustainable, federated database for members of clinical and translational research study teams to share and access training and assessment resources.
This session outlines the process of obtaining valid informed consent and will give you the opportunity to demonstrate necessary language and communication skills when interacting with potential study participants and their families.