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Humanitarian Use Device (HUD) Informed Consent Template

This template should be used when submitting the Humanitarian Use Device (HUD) informed consent documents. The Food and Drug Administration (FDA) defines a Humanitarian Use Device (HUD) as “a medical device intended to benefit patients in the...

Guidance

May 11, 2020

Humanitarian Use Device Requirements for U-M Physicians & Investigators

The Food and Drug Administration (FDA) defines a Humanitarian Use Device (HUD) as “a medical device intended to benefit patients in the treatment or diagnosis of a disease or condition that affects or is manifested in not more than 8,000 individuals...

Guidance

Mar 27, 2020

Informed Consent Procedures Using Electronic Systems and Remote Use of Paper Documents

Updated April 9, 2020 Electronic and remote informed consent procedures are permitted by IRBMED and must meet the same regulatory and institutional requirements of an in-person paper-based informed consent process. This guidance is intended for...

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Guidelines

May 1, 2019

Guidelines on Anesthesia and Analgesia in Dogs

This document has been designed by the ULAM veterinary staff as a guideline for sedation , anesthesia , and analgesia of laboratory canines. This is not intended to be an inclusive tutorial on all possible drug combinations that can be used in...

SOPs

Feb 1, 2013

Procedures for Campus-Wide Fur Mite Treatment

This document provides an overview of the procedures necessary for the coordinated fur mite treatment of all of the mouse and rat colonies at the University of Michigan Ann Arbor campus. This document also describes procedures needed for quarantine...

Policies

Jun 17, 2017

University of Michigan Medical School Central Biorepository Policy Acknowledgment and Authorship

It is important to recognize the University of Michigan Medical School (UMMS) Central Biorepository (CBR) and the Principal Investigators who collect research materials for the contributions they make to scientific advancement of projects utilizing...