using language appropriate to your specific research, setting, and participants. There is no need to utilize the UAB IRB’s Sample Consent form for consent processes in exempt research. Your consent ...

and what rights they have as research subjects. The consent form is one part of the dialogue that investigators have with each subject. It is recommended that forms for adult subjects be written at a ...

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 ...

The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project.

Note: The IRB must be provided with “sponsor verification” in the form of a letter signed by the sponsor(s) with the same wording given in the consent form ... may result from participation in the ...