8 found
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  1. Child’s Objection to Non-Beneficial Research: Capacity and Distress Based Models.Marcin Waligora, Joanna Różyńska & Jan Piasecki - 2016 - Medicine, Health Care and Philosophy 19 (1):65-70.
  2.  2
    Regulation of Healthcare Ethics Committees in Europe.Norbert Steinkamp, Bert Gordijn, Ana Borovecki, Eugenijus Gefenas, Jozef Glasa, Marc Guerrier, Tom Meulenbergs, Joanna Różyńska & Anne Slowther - 2007 - Medicine, Health Care and Philosophy 10 (4):461-475.
    In this article, the question is discussed if and how Healthcare Ethics Committees (HECs) should be regulated. The paper consists of two parts. First, authors from eight EC member countries describe the status quo in their respective countries, and give reasons as to the form of regulation they consider most adequate. In the second part, the country reports are analysed. It is suggested that regulation of HECs should be central and weak. Central regulation is argued to be apt to improve (...)
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    Emergency Research Without Consent Under Polish Law.Joanna Różyńska & Marek Czarkowski - 2007 - Science and Engineering Ethics 13 (3):337-350.
    Although Directive 2001/20/EC of the European Parliament and of Council of 4 April 2001 on the approximation of the laws regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use does not contain an exception for emergency situations, and requires the informed consent of a legal representative in all cases where research is conducted on legally competent individuals who are unable to give (...)
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    Racje sumienia a inne powody odmowy wykonania świadczenia zdrowotnego przez lekarza.Joanna Różyńska & Jakub Zawiła-Niedźwiecki - 2016 - Medycyna Praktyczna - Psychiatria 2 (49):74-83.
  5. Wspomagane umieranie w psychiatrii – dlaczego nie?Jakub Zawiła-Niedźwiecki & Joanna Różyńska - 2016 - Psychiatra 2:18-20.
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    On the Alleged Right to Participate in High‐Risk Research.Joanna Różyńska - 2015 - Bioethics 29 (7):451-461.
    Reigning regulatory frameworks for biomedical research impose on researchers and research ethics committees an obligation to protect research participants from risks that are unnecessary, disproportionate to potential research benefits, and non-minimized. Where the research has no potential to produce results of direct benefit to the subjects and the subjects are unable to give consent, these requirements are strengthened by an additional condition, that risks should not exceed a certain minimal threshold. In this article, I address the question of whether there (...)
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  7. Środowiskowe Przyzwolenie Na Łamanie Zasad Dobrej Praktyki Badawczej W Opinii Społeczności Akademickiej.Witold Rekowski, Alicja Przyłuska-Fiszer, Joanna Różyńska & Barbara Fijałkowska - 2012 - Zagadnienia Naukoznawstwa 48 (194).
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  8. Złe geny, „złe życie” i koncepcja krzywdy progowej.Joanna Różyńska - 2013 - Etyka 47.
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