There has been an increased focus over the past couple of years on patient rights, resulting in a renewed emphasis on informed consent by healthcare regulators, such as The Joint Commission. This ...

Obtaining a patient’s consent is not the same as having a patient sign a consent form. While a written, countersigned document provides important evidence if consent is disputed in court, in order for ...

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 ...

Increasingly, medical procedures in the United States are being performed in ASCs. According to statistics released earlier this year, the Centers for Disease Control and Prevention’s National Center ...

It's time to revise the informed consent process and create a reasonable-patient standard through shared decision-making between physicians and patients, according to a viewpoint piece in the Journal ...

The Agency for Healthcare Research and Quality teamed up with the Joint Commission and Abt Associates to offer free online courses for hospital leaders and others to learn how to improve the patient ...

Research participants have commonly been found to lack basic understanding of fundamental aspects of the studies in which they are participating. The informed consent process is one of many aspects of ...

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.

A survey of patients receiving treatment in a teaching facility found that patients prefer to be informed of trainee participation in their care, and consent rates appear to vary based on scenarios ...

Over one million hematopoietic cell transplants have been performed worldwide since the first report of successful hematopoietic cell transplant in 1957. In current medical practice, hematopoietic ...