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.

Legally effective informed consent will be obtained from the participant or the participant's legally authorized representative prior to including the participant in research. Informed consent will be ...

Obtaining informed consent is a basic ethical obligation and a legal requirement for researchers. This requirement is founded on the principle of respect for persons. Potential participants must be ...

Sexting – the creating and exchanging of sexual texts, photos and videos – has become part of many people’s sexual and ...

Exception From Informed Consent Research 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 ...

Informed consent for non-exempt research must almost always be obtained in writing, and the regulations are explicit about the elements that must be included. Consent requirements can be waived by the ...

Review of Informed Consent for Exempt and Qualifying Minimal Risk Research Research Integrity & Security staff (for exempt research) and IRB members (for qualifying minimal risk research) will assess ...

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 ...

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.

Informed Consent Process It is the policy of Western Michigan University that all research involving human subjects will be reviewed by the Institutional Review Board. The involvement of human ...

Informed consent (IC) is a fundamental aspect of ethical clinical research, safeguarding the rights and well-being of participants. It empowers participants with comprehensive information about the ...

Trial sponsors have struggled to improve trial diversity. Homing in on informed consent may be the key to changing that—with the welcome side effect of empowering patients to participate in ...