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 ...

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

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 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 ...

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 ...

The use of deception or incomplete disclosure limits the subject's ability to make a fully informed decision of whether to participate in the research — one of the essential ethical concerns in human ...

Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that ... benefit to the research subjects, and the child’s age, maturity, status, ...

See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2 ... and their probability as a direct result of participation in the research and/or from breach ...

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.