Past Events

We are in a new era of research transparency which requires advance planning for data sharing. In this virtual session, participants will learn how to put together National Institutes of Health (NIH) data management & sharing (DMS) Plans, how to harmonize informed consent language with DMS Plans, and, if needed, how to translate the NIH […]

The Michigan Institute for Clinical and Health Research (MICHR) Mock Study Section is an opportunity to practice thinking like an NIH grant reviewer on a mock “study section.” As one of six grant reviewers, you will discuss actual twelve-page K and R grants (already submitted in some version to the NIH). You will practice for […]

The Michigan Institute for Clinical & Health Research (MICHR) invites early-career faculty and experienced researchers new to the University to attend Orientation for Clinical Investigators. This orientation will provide an overview of the information, resources, and tools needed to comply with clinical research regulations and help you navigate the University’s research enterprise efficiently. This 3-hour […]

We are in a new era of research transparency, which means our study documentation must be clearer than ever. A significant part of this transparency is ClinicalTrials.gov, which has evolved since its inception years ago and is changing the way we think about measuring and reporting data outcomes. In this interactive, virtual session, participants will […]

This workshop outlines the process of obtaining valid research-informed consent and will give you the opportunity to demonstrate necessary language and communication skills when interacting with potential study participants and their families. This session is not about writing the informed consent document or specific U-M IRB requirements. Attendees of the workshop should come prepared for […]

This interactive, virtual session will introduce participants to best practices for procedures documentation to ensure standardized practices across personnel and sites of a clinical trial. While we will touch on several methods for documentation, the workshop will mainly focus on creating, interpreting, and using a manual of procedures (MOP). Topics include an overview of the […]

In this workshop, you will learn best practices in preparing for a new study before you submit an IRB application or for beginning a new phase of the research. You’ll get expert tips from an experienced coordinator that will help you save time, effort and money later in your study. This engaging session will include […]

Beyond Accreditation: Defining Drives of Cancer Quality Improvement in a Statewide Learning Health System Dr. Calista Harbaugh, MD, MS Assistant Professor of Surgery Associate Chair, Department of Surgery Medical School Our joint Implementation Science Incubator session with the Center for Healthcare Outcomes & Policy (CHOP) is approaching. Please join us on Friday, July 17, from […]

This workshop 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. This session is not about writing the informed consent document or specific U-M IRB requirements. Attendees of the workshop should come prepared for […]

Join us for an interactive introduction to best practices in preparing for and participating in clinical trial monitoring visits. During this virtual program you will learn about the purpose of monitoring and how it differs from an audit, what to expect from different types of monitoring visits, preparing for an interim visit, and tips on […]