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 ...

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 ...

The informed consent model of care is based on providing accurate and in-context information so that you can make the best decision about your healthcare plan. When people talk about options for ...

Human clinical trials are the final stage of research for any new medical treatment. Medical breakthroughs rely on willing participation from people who agree to be part of the studies. Joining a ...

The principle of respect for persons demands that participants enter the research voluntarily and with adequate information. When deceptive methodologies are used, participants are given incomplete or ...

A lot has been written about ensuring that the language of informed consent forms is at a level that is easily understandable, and for good reason. The Food and Drug Administration requires all ...

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 ...

David Blakeney died in a nursing home. Mr. Blakeney was a 63-year-old nursing home resident with dementia who died eight months after being prescribed an antipsychotic drug to address behaviors ...

In their article, Smith and Mackie argue that vaccine mandates do not impair the voluntariness of informed consent, even when ...

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 ...