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.

The informed consent model involves healthcare professionals providing information to people so they can make informed decisions about their own healthcare. For transgender adults, this model ...

The latest word, according to Stat, is that the Department of Health and Human Services directed the CDC to curtail vaccine advertising and focus on informed consent. So, just what does that mean?

The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed consent process. Investigators can avoid delay in the review process ...

Study results suggest that “telemedicine represents a unique opportunity to reduce time and travel burdens for patients with cancer considering clinical trials,” according to researchers.

Obtaining the informed consent of a potential human subject for participation in any research (whether an experiment, survey, interview, or demonstration) is a federally mandated safeguard for ...

This amendment required patients to provide "informed consent" before participating in drug studies. The new standards would go on to change not only the way Americans participated in drug trials ...