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 ...

Many consent forms are not as good as they could be in terms of aiding decision-making. ... Non-Exempt Research Informed Consent Example. Address and Phone. University Services Center, 87-2400 141 ...

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

You're required to have all participants in your study complete an Informed Consent Form. See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s ...

Department of Health and Human Services (DHHS) regulations for the protection of human participants require that informed consent information be presented in language understandable to the participant ...

However, some situations are more likely to require informed consent, for example when an identifiable member of the public is shown receiving medical treatment. (See Guidance: Filming in Medical ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...

Certinal has announced the launch of its new Consent Form Management System (CFMS), offering hospitals a modern solution to ...

On July 19, the Florida Board of Education modified the Florida Administrative Code Rule 6A-1.0955, which now requires written parental consent for using student names other than their legal names.