The goal of this requirement is to increase transparency for federally funded clinical trials and simultaneously create a repository of sample consent forms that may be used as a reference for future ...

The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the format that we ...

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 European Union’s General Data Protection Regulation requires every organization that collects sensitive personal data from those residing in the EU to ask for clear and specific consent ...

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 ...