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, ...

If the research is sponsored ... consent documents rather than a separate informed consent document including the following choices: Limiting use for specified diseases; Allowing unlimited use; ...

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 ...

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 ...

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 ...

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.

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 ...

The Tuskegee syphilis study, also known as the U.S. Public Health Service (USPHS) Untreated Syphilis Study at Tuskegee, is one of the most infamous chapters in the history of U.S. public health and ...

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, ...

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.