A signed informed consent form notifies potential research participants of their obligations and ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

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: ...

secure the written informed consent of any human subject used in research before involving that subject in the research project. In preparing instructions for subjects being asked to sign this consent ...

Informed consent ... the nature of the research project, why they are candidates for the research, what risks, benefits, and alternatives are associated with the research, and what rights they have as ...

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.

Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that ... benefit to the research subjects, and the child’s age, maturity, status, ...

Note: The IRB must be provided with “sponsor verification” in the form of a letter ... about any research that involves the collection of identifiable private information or identifiable biospecimens: ...

Obtaining informed consent for participation in medical research is particularly ... and informed-consent text, in the form of templates and sample forms. We surveyed U.S. medical schools to ...

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

Informed consent provides the individual with the pertinent information regarding the research in which s/he is being asked to participate, and the opportunity to make an informed decision regarding ...

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 ... and ...