Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, provided the conditions described on the waiver form are fulfilled.

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website ... clinical trials and simultaneously create a repository of sample consent forms ...

A waiver of the need for subjects to sign a consent form can be granted if any one of the following three conditions are met: The only record linking the subject and the research would be the consent ...

Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...

Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that the form is written ... and condition. This sample is intended to help you ...

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...