The Forms and Templates page includes templates for informed consent documents. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

The federal regulations for the protection of human subjects (Common Rule) were revised effective January 20, 2019 to reduce administrative burdens for low-risk research while enhancing protections ...

Informed consent has been defined as "an ... [2,3] Beyond providing information to patients and potential research participants, it is important that the physician or investigator assesses the ...

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 ...

You're thinking of participating in a clinical trial – what now? Ask questions and weigh the risks before deciding if a clinical trial is right for you.

Informed consent documents explain to potential participants the information that a reasonable ... this includes: the nature of the research project, why they are candidates for the research, what ...

The investigator should, normally, explain all other aspects of the research or intervention about which the participants enquire. Failure to make full disclosure prior to obtaining informed consent ...

Manuscripts must also include a statement affirming that informed consent was obtained from all human research participants. Additionally, we require that all content submitted for publication be ...

Generally, trial participants receive an 'informed consent' document providing information ... To avoid such conflicts, the Office for Human Research Protections, the division of the US government ...

Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.