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 ...

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.

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

The authors highlight that informed consent and ethical approval are distinct ethical responsibilities. The former ensures ...

Click here to watch a short video on what is Exception From Informed Consent research. Acute care research is sometimes conducted under Exception from Informed Consent regulations. In many ...

Informed consent is an agreement between the investigators and the ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...