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 ...

Informed consent is a process that’s required for most medical procedures. However, there’s often confusion about what informed consent is, what it means, and when it’s needed. In a healthcare setting ...

A team of Northwestern Medicine investigators recently began developing a library of visual icons to support research participant comprehension of informed consent forms.

Although informed consent for clinical treatment has become a vital part of contemporary medical practice, it means different things in different contexts (Figure 1), is variably practised and rarely ...

In her Health Affairs Blog post last fall, Sharon Brownlee lamented how frequently patients agree to treatments that they know little about. In the United States and elsewhere, clinicians have a clear ...

This is the second in a series of articles that focuses on your rights as a patient—both inside the hospital and out. First up, we explored the Patient’s Bill of Rights (yes, that’s a thing!). Today ...

Obtaining informed consent is a basic ethical obligation and a legal requirement for researchers. This requirement is founded on the principle of respect for persons. Potential participants must be ...

Forbes contributors publish independent expert analyses and insights. Diane Omdahl is a Medicare expert who keeps her readers in the know. Anyone who has had an MRI, a surgical procedure or even a ...

Achieving informed consent requires a potential contributor to be in possession of sufficient knowledge about our plans for a reasoned decision to take part in our content. The Editorial Guidelines ...