Once consent forms are approved, they will be "stamped." The stamped versions must be used when consenting participants. Templates & Types of Informed Consent . Click on each header below to learn ...

Consent Form Templates The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating ...

Note that with this new template informed consent forms will no longer be stamped with an expiration date. The documents will still have an IRB approved date which will be located in the header of the ...

The IRB Office published an updated version of the informed consent template. The template and instructions for uploading this form in eRA have been posted to the Forms & Templates page.. For your ...

Several sections under General Information contain guidance about consent and assent: IRB-Review—Outcomes-and-Approval-Details; Conducting the Protocol; Participant Populations; The UAB IRB also ...

Institutions as diverse as the National Cancer Institute and the State University of New York Downstate Medical School have presented informed-consent templates and sample forms that are below an ...

Informed consent forms for interventional oncology clinical trials are often lengthy and written at too high of a reading level for some patients, making it hard for them to weigh the decision to ...

In this study, all of the consent forms were based on templates provided by the funder, ... (2011, July 20). Informed-consent forms should be shortened, simplified, bioethicists say. ScienceDaily.

Defines informed consent; Outlines where to find the most up-to-date consent form template, the HRP-502; Identifies the parts of the Informed Consent form; Shares how to deliver information to ...