Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

Therefore, the IRB will very carefully review the method of obtaining and the content of informed consent listed below. When consent forms require signatures of research subjects and/or their parents ...

Informed consent documents explain to potential participants the information that a reasonable person would want to have in order to make an informed decision about whether to participate. Using this ...

No protocol, informed consent process, or informed consent document may be modified without prior approval from the IRB unless it is necessary to eliminate an apparent and immediate hazard to one or ...

Arguments in a legal challenge brought by an abortion rights group in Michigan began Thursday as the group looks to eliminate ...

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 ...

A civil trial opened Thursday on a challenge to abortion restrictions that remain on the books in Michigan. We have more from ...

Abortion providers had sued the state last year, arguing a ballot proposal passed in 2022 makes certain abortion restrictions unconstitutional.

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 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, ...

It is important to remember that informed consent is an ongoing process, not a document or single event. An investigator should seek informed consent only under circumstances that: provide the ...