Patient Consent: Defining Control of Genetic Information
نویسندگان
چکیده
منابع مشابه
SOP 05: Patient information and informed consent.
Adequate patient information with particular emphasis on the fact that participation in the study is voluntary is a particular concern of the ‘Declaration of Helsinki’ [1] and Guidelines on Good Clinical Practice. Great care must therefore be taken in formulating and adapting a written patient information sheet to the particular requirements of a given study. The written patient information mus...
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BACKGROUND Before participation in medical research an informed consent must be obtained. This study investigates whether the readability of patient information and consent documents (PICDs) corresponds to the average educational level of participants in rheumatological studies in the Netherlands, Denmark, and Norway. METHODS 24 PICDs from studies were collected and readability was assessed i...
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Physicians have always strived to uphold all the ethical postulates of the medical profession in all aspects of the practice, however with the vast advances in science and technology, numerous ethical dilemmas regarding all aspects of life and ultimately death have emerged. Medical decisions however, are no longer in the sole jurisdiction of traditional Hippocratic medicine but are now delibera...
متن کاملGuidelines for researchers: patient information sheet and consent form.
The guidance, which follows, applies primarily to multi-centre pharmaceutical studies and encompasses the ICH Good Clinical Practice guidelines. However, the principles and much of the content will be of use to researchers writing information sheets in their particular fields, for trials involving patients, patient volunteers and healthy volunteers. You will find it helpful to refer also to oth...
متن کاملIntegrating Patient Consent in e-Health Access Control
Many initiatives exist that integrate e-health systems on a large scale. One of the main technical challenges is access control, although several frameworks and solutions, like XACML, are becoming standard practice. Data is no longer shared within one affinity domain but becomes ubiquitous, which results in a loss of control. As patients will be less willing to participate without additional co...
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ژورنال
عنوان ژورنال: JNCI: Journal of the National Cancer Institute
سال: 2017
ISSN: 0027-8874,1460-2105
DOI: 10.1093/jnci/djx170