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.

Warning! Sweeping changes in public health are on the rise. The latest word, according to Stat, is that the Department of ...

The failure of Panhandle Health District board members to honestly address how patients are informed of the risks and benefits of vaccine products at the March 3 PHD meeting reveals a troubling ...

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 ...

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 ...