Results 61 to 70 of about 3,084,357 (186)
Informed consent of children in field trials. [PDF]
, 1979 S. Stephen Kegeles, A K Lund
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Resuscitation PlusBackground: No previous study has evaluated patients attitudes towards inclusion in an ongoing cardiac arrest clinical trial. The aim of this study was to assess patientś willingness and motives to participate in the ongoing randomized controlled drug ...
Malin Albert +12 more
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Implementing ISO/IEC TS 27560:2023 Consent Records and Receipts for GDPR and DGA [PDF]
arXivThe ISO/IEC TS 27560:2023 Privacy technologies - Consent record information structure provides guidance for the creation and maintenance of records regarding consent as machine-readable information. It also provides guidance on the use of this information to exchange such records between entities in the form of 'receipts'.
arxiv
The validity of informed consent in a clinical study [PDF]
, 1984 Neville W. Goodman +3 more
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Why the British courts rejected the American doctrine of informed consent (and what British physicians should do about it). [PDF]
, 1984 George J. Annas
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Informed Consent in Biomedical Research
Computational and Structural Biotechnology Journal, 2019 Informed consent is the result of tumultuous events in both the clinical and research arenas over the last 100 years. Throughout this time, the notion of informed consent has shifted tremendously, both due to advances in medicine, as well as the type of ...
Fida K. Dankar +2 more
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Empowering Patients for Disease Diagnosis and Clinical Treatment: A Smart Contract-Enabled Informed Consent Strategy [PDF]
Communications in Computer and Information Science (CCIS) 2024Digital healthcare systems have revolutionized medical services, facilitating provider collaboration, enhancing diagnosis, and optimizing and improving treatments. They deliver superior quality, faster, reliable, and cost-effective services. Researchers are addressing pressing health challenges by integrating information technology, computing resources,
arxiv
INFORMED CONSENT – RIGHT OR BURDEN
Zdravniški Vestnik, 2016 Informed consent is legal institute that was introduced in the research area to prevent possible abuses in human research. Almost a century later it was introduced also in general medicine outside the research area.
Borut Stražišar, Branka Stražišar
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