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 ...

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, ...

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 ...

8. Acknowledgment and Consent By signing below, you acknowledge that you have read and understood this informed consent document. You agree to the terms outlined and consent to receive mental health ...

Keep in mind that obtaining informed consent is a continuous process throughout the research, not simply a one-time event when a subject signs a form. To ensure informed consent, researchers should: ...

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 ...

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, ...

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 ...

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 ...

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 ...