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Standard Informed Consent Template

New IRBMED studies should most often use the latest Standard Informed Consent template available on this webpage. Specialty Consent Templates may be appropriate for low-risk studies with simpler study methodologies.

Guidance

Jun 7, 2021

Other Reportable Information or Occurrence (ORIO)

Investigators sometimes receive information that has a direct impact on a research study. This information is reportable to the IRBMED . Frequently this information falls within the Adverse Event Reporting context, or it is reported to IRBMED in...

Guidance

Jun 4, 2021

Information Blocking in a Blinded Study

Single Blind Studies : A research study done in such a way that the participants do not know (are blinded to) what treatment they are receiving to ensure the study results are not biased (the power of suggestion). Blinded studies are sometimes...

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SOPs

Feb 26, 2021

Environmental Enrichment for Animals SOP

This document outlines the use and approval of environmental enrichment for all vertebrate animals.

Guidelines

Nov 27, 2019

Anesthesia and Sedation Monitoring Guidelines

This document was created by the ULAM veterinary staff as a guideline for anesthesia and sedation monitoring. This is not intended to be an inclusive tutorial on all possible methods and all equipment available for anesthesia monitoring. Detailed...

Policies

Apr 1, 2013

Service Policy on Submitting* PHS Proposals

This policy describes the service level delivery that will be provided by Grant Services & Analysis in the Medical School when submitting PHS proposals. Service levels are determined by the number of days in advance of the deadline the finalized...