2012

Human Medical Research

Ethical, Legal and Socio-Cultural Aspects

ISBN: 978-3-0348-0389-2 (Print) 978-3-0348-0390-8 (Online)

Table of contents (15 chapters)

  1. Front Matter

    Pages i-xv

  2. No Access

    Book Chapter

    Pages 1-4

    Introduction

  3. Historical and Socio-Cultural Contexts in Medical Research

    1. Front Matter

      Pages 5-5

    2. No Access

      Book Chapter

      Pages 7-17

      British Responses to Nazi Medical War Crimes

    3. No Access

      Book Chapter

      Pages 19-28

      History and its Relevance in the Development and Teaching of Research Ethics

    4. No Access

      Book Chapter

      Pages 29-41

      Human Embryo Research and Islamic Bioethics: A View from Iran

    5. No Access

      Book Chapter

      Pages 43-51

      From Farming to Pharming: Transcending of Bodily Existence as a Question of Medical Ethics in an Intercultural Context

  4. Considerations on Ethical and Legal Regulations for Medical Research

    1. Front Matter

      Pages 53-53

    2. No Access

      Book Chapter

      Pages 55-63

      Rethinking the Therapeutic Obligation in Clinical Research

    3. No Access

      Book Chapter

      Pages 65-86

      Biomedical Research in Developing Countries and International Human Rights Law

    4. No Access

      Book Chapter

      Pages 87-96

      Research Involving Human Subjects and Human Biological Material from a European Patent Law Perspective. Autonomy, Commodification, Patentability

    5. No Access

      Book Chapter

      Pages 97-114

      The Development and Validation of a Guide for Peruvian Research Ethics Committees to Assist in the Review of Ethical-Scientific Aspects of Clinical Trials

  5. Conflicts in Medical Research

    1. Front Matter

      Pages 115-115

    2. No Access

      Book Chapter

      Pages 117-126

      Conflicts of Interest in Medical Research: What can Ethics Contribute?

    3. No Access

      Book Chapter

      Pages 127-136

      Research Ethics in Genomics Research: Feedback of Individual Genetic Data to Research Participants

    4. No Access

      Book Chapter

      Pages 137-151

      Regulating “Higher Risk, No Direct Benefit” Studies with Children: Challenging the US Federal Regulations

  6. New Developments in Medical Research and Ethical Implications

    1. Front Matter

      Pages 153-153

    2. No Access

      Book Chapter

      Pages 155-162

      A Paradigm Change in Research Ethics

    3. No Access

      Book Chapter

      Pages 163-173

      Translation of Cancer Molecular Biomarkers: Ethical and Epistemological Issues

    4. No Access

      Book Chapter

      Pages 175-184

      Rethinking the Ethics of Human Biomedical Non-Interventional Research

  7. Back Matter

    Pages 185-188