منابع مشابه
Normative consent is not consent.
The UK has an opt-in system of consent for postmortem organ donation. More specifically, the Human Tissue Act 2004 prohibits the removal, storage, and use of organs postmortem for a range of ‘‘scheduled purposes’’—which include transplantation—unless ‘‘appropriate consent’’ has been given. Appropriate consent can be given by the donor premortem by signing and carrying a donor card, or by opting...
متن کاملConsent.
The State Board of Education meeting was held on Thursday, September 18, 2014, in the Grimes State Office Building, State Board Room, Des Moines, Iowa. The following State Board members were present: Charlie Edwards, Mike Knedler, Rosie Hussey, Mike May, Mike Bearden, Diane Crookham-Johnson, Brooke Axiotis, Mary Ellen Miller, Angela English, and Hannah Rens. Iowa Department of Education staff m...
متن کاملAdherence to Informed Consent Standards in Shiraz Hospitals: Matrons Perspective
Background Informed consent is an important part of the patients’ rights and hospitals are assigned to obtain informed consent before any diagnostic or therapeutic procedures. Obtaining an informed consent enables patients to accept or reject their care or treatments and prevent future contentions among patients and medical staff. Methods This survey was carried out during 2011-2. We assessed...
متن کاملUnderstood Consent Versus Informed Consent: A New Paradigm for Obtaining Consent for Pediatric Research Studies
All too often the informed consent process is viewed by members of research teams as a challenge of getting a parent or young person's signature on a form. Informed consent is, however, much more than a signed form. Rather, it is a process, often iterative, in which the parent or young person is given sufficient information about a study in order that they can make a truly informed decision abo...
متن کاملBeyond the informed consent procedure: continuing consent in human research.
An ethnographic field study about informed consent in hepatitis C clinical trials provides insight into how changes in protocol requirements and patient health status triggered the actions and decisions of researchers and human subjects during the conduct of these trials. U.S. federal guidelines recommend that informed consent should be conceptualized as more than a one-time event. Rather, a pr...
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ژورنال
عنوان ژورنال: Journal of Universal College of Medical Sciences
سال: 2014
ISSN: 2350-8582,2091-2846
DOI: 10.3126/jucms.v1i4.9581