There is no need to utilize the UAB IRB’s Sample Consent form for consent processes in exempt research. Your consent process should be clear and contain full sentences that are in no more than 8th ...

See the Informed Consent Template for an example of informed consent at the eighth grade reading level. (For additional help, see Readability Tools below.) When using an informed consent form, a final ...

The Informed Consent Form should be in the primary language of the research participant, or at least in a language in which the participant is considered fluent. The investigator should submit a ...

For example, the informed consent for a research study might advise patients in the following way: Over the course of this trial, routine healthcare information, such as [name of test] results and ...

When audio- or video-recording your participants while conducting research, you must specifically ask your participants' consent to be recorded prior to having them sign the consent form. Sample ...

See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s elements of informed consent for research with humans. Please also consult the Federal ...

326. Short Form Written Consent Documentation | Research Integrity & Security | University of Nevada, Reno ...

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.

Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

Clinical research consent forms for certain FDA-regulated clinical trials are now required to contain a specific statement advising participants that clinical trial information will be entered ...