Patients’ Rights: Informed Consent

Informed consent and patients' rights in Japan.

Patients, agents, and informed consent.

Informed consent, confidentiality, and subject rights in clinical trials.

The informed consent process is designed to inform the subject of the risks, rights, and benefits of participation in a clinical research trial. Informed consent, while not always necessary, is a critical component of ethical research involving human subjects. This article includes an overview of two sets of regulations regarding informed consent found in the Code of Federal Regulations (CFR) T...

preoperative informed consent: is it truly informed?

background: pre-operative informed consent is an important aspect of surgery, yet there has been no formal training regarding it in pakistan. this study was done to assess the preoperative informed consent practice. methods: after taking informed permission, a questionnaire was filled in during an interview with 350 patients, who have undergone elective surgical procedures under routine practic...

When is Informed Consent “Informed”?

Typically, a consent document in the United States is a printed form with blank spaces in which the operative procedure is filled in. The form is signed by the patient, and placed into the medical record. At first glance, it would seem that the patient was told of the operative procedure and gave his or her consent. Yet informed consent, or, more accurately, lack of informed consent, is a frequ...