Can informed consent to research be adapted to risk? - Wikidata - awgldk - TriplyDB

Can informed consent to research be adapted to risk?

Can informed consent to research be adapted to risk?

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Use of altered informed consent in pragmatic clinical research.Autonomy and Fear of Synthetic Biology: How Can Patients' Autonomy Be Enhanced in the Field of Synthetic Biology? A Qualitative Study with Stable Patients.First-in-human HIV-remission studies: reducing and justifying risk.

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Can informed consent to research be adapted to risk?

http://www.wikidata.org/entity/Q51776330

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2014 nî lūn-bûn

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Can informed consent to research be adapted to risk?

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Can informed consent to research be adapted to risk?

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MEDETHICS-2013-101912

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Journal of Medical Ethics

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Can informed consent to research be adapted to risk?

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Danielle Bromwich

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Informed consent, comparative effectiveness, and learning health care

Is informed consent always necessary for randomized, controlled trials? .

What makes clinical research ethical?

The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countries

Animal derived products may conflict with religious patients' beliefs.

Readability standards for informed-consent forms as compared with actual readability.

Are there adverse consequences of quizzing during informed consent for HIV research?

Helping patients decide: ten steps to better risk communication.

Communication and informed consent in phase 1 trials: a review of the literature.

Analysis of informed consent document utilization in a minimal-risk genetic study

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521-528

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scholarly article

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10.1136/MEDETHICS-2013-101912

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7

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41

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informed consent