Federal regulations require that researchers obtain legally effective, documented, voluntary informed consent from prospective subjects (or subjects' legally authorized representatives) before ...

Informed consent is a fundamental component of modern healthcare and represents a patient's right to understand and agree to a medical procedure, treatment or study. True informed consent empowers ...

Informed consent represents one of the most important ethical aspects of clinical treatments and scientific research involving humans. This article will discuss the key elements of informed consent ...

It can be a rewarding experience to participate in research studies that offer many potential personal, medical, and financial benefits. However, if you are new to or are not entirely familiar with ...