Results 31 to 40 of about 3,654,357 (349)
, 2019 Activities on privacy, safety, and ethics are of course an essential part of the IPAR-UCD approach to make it transversal to the entire work plan to ensure that issues are supervised and handled professionally alongside all activities with users. Managing privacy, safety and ethics are core reach objectives of IPAR (and not an “add-on”).
Bosse, Ingo +2 more
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How informed are you about informed consent?
Indian Journal of Vascular and Endovascular Surgery, 2019 The past decade has seen a rise in the awareness of patients, and their attendants have about their disease, options for treatment and their legal rights, thanks to easy access to the Internet, however accurate it may be. Surgeons need to be aware of the
Edwin Stephen
doaj +1 more source
An integrated conceptual framework for evaluating and improving ‘understanding’ in informed consent
Trials, 2017 Background The development of understandable informed consent (IC) documents has proven to be one of the most important challenges in research with humans as well as in healthcare settings.
Sabine Bossert, Daniel Strech
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Improving assent in health research: a rapid systematic review
BMC Medical Research Methodology, 2020 Background Enrolment in a research study requires the participant’s informed consent. In the case of minors, informed consent of the respective legal guardian is obtained in conjunction with informed assent of the underage p articipant.
Dominik Soll +3 more
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Etikk i Praksis: Nordic Journal of Applied EthicsThis article reflects on the central themes of Vilhjálmur Árnason's work, particularly his focus on contextualized morality and dialogical ethics.
Vilhjalmur Arnason
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Southern African Journal of HIV Medicine, 2001 No abstract available.
Steve Andrews
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Quality of informed consent in clinical trials
Journal of Pre-Clinical and Clinical Research, 2020 Introduction and objectives Obtaining consent prior to any medical intervention is currently a necessity, the omission of which may lead to litigation. Years of analyses have resulted in strict policies as to what should the patient be informed about and
Anna Zagaja
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Informed Consent and Consent Forms [PDF]
The Permanente Journal, 2008 Informed consent is not often a significant part of a malpractice claim. To prevail on this issue, a jury or arbitrator must be convinced that the claimant would not have agreed to undergo the procedure if the possibility of occurrence of the complication that ultimately occurred, no matter how rare, had been disclosed.
openaire +3 more sources
Voices in Bioethics, 2014 Biobanks have added complexity to the idea of informed consent, which is an important ethical component in research involving human subjects. The idea behind informed consent is that each potential participant needs to voluntarily determine whether or ...
Gabriella Foe
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Voices in Bioethics, 2013 In America, with our closely held values of optimism and perseverance, we are very often loath to confront death and dying; cancer patients are told to fight, to hold on to a positive attitude, to nurture faith and hope.
Jennifer Cable
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