Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, provided the conditions described on the waiver form are fulfilled.

Informed consent is a foundational element of every clinical trial. Yet, the traditional paper-based process has long been ...

Informed consent is vital for any clinical trial. However, the length and complexity of consent information can lead to patients misconstruing key points and failing to understand the implications ...

"In addition to clinical consequences, should informed consent include a discussion of the non-medical consequences?" ...

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research participants of their obligations and rights, and ...