Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

Defines informed consent; Outlines where to find the most up-to-date consent form template, the HRP-502; Identifies the parts of the Informed Consent form; Shares how to deliver information to ...

The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project.

Potential research subjects must be accurately informed of what a project involves, and given the opportunity to decide of their own free will whether or not to participate. This process may be brief ...

Moving forward, making informed consent truly informed – rooted in both equity and accessibility –  needs to be a priority, ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...