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 ...

Acute care research is sometimes conducted under Exception from Informed Consent regulations. In many life-threatening illnesses, patients are unconscious or too sick to provide written or verbal ...

A successful consent process presents detailed information which is organized and presented in a way that helps the prospective subject understand why a person might or might not want to participate.

Informed consent involves a subject being given information that a reasonable person would want to have to make an informed decision about whether to participate in research, and the chance to discuss ...

The United States Health and Human Services Department (HHS) published a landmark report on intersex health equity last week, ...

Find out some dementia-friendly ways of ensuring consent is valid, when you are doing research with people affected by dementia. Traditional approaches to ensuring informed consent may be too reliant ...

A doctor's visit often ends with you leaving with a pathology request form in hand. The request form soon has you filling a sample pot, having blood drawn, or perhaps even a tissue biopsy taken.

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.

See the informed consent form template (pdf ... risk or harms to the subject and their probability as a direct result of participation in the research and/or from breach of confidentiality. (Remember: ...

Furthermore, unless the consent process has been specifically waived by the IRB, no subjects may be included in research unless the investigator has obtained the legally effective informed consent of ...