Ethics and Governance of Biomedical Research (eBook)

Theory and Practice

Daniel Strech, Marcel Mertz (Herausgeber)

eBook Download: PDF

2016 | 1st ed. 2016
VIII, 225 Seiten
Springer International Publishing (Verlag)
978-3-319-28731-7 (ISBN)

Infos

In this book, scholars with different disciplinary and national backgrounds argue for possible answers and analyse case studies on current issues of governance in biomedical research. These issues comprise among others the research-care distinction, risk evaluation in early human trials, handling of incidental findings, nocebo effects, cluster randomized trials, publication bias, or consent in biobank research. This book demonstrates how new technologies and research possibilities multiply or intensify already known governance challenges, leaving room for ethical analysis and complex moral choices. Clinical researchers, research ethics committee members and research ethicists have all to deal with such challenges on a daily basis. While general reflection on core concepts of research ethics is seldom pointless, those confronted with hard moral choices do need more practical and contextualized reflection on the said issues. This book particularly provides such contextualized reflections and aims to inform all those who study, conduct, regulate, fund, or participate in biomedical research.

Inhalt

Introducing new domains of research governance; Govind C. Persad, JD,
BS, BA.- Should Research Ethics Encourage the Production of Cost-Effect Interventions?; Rebecca Johnson, MA.-  From altruists to Workers: What
Claims Should Healthy Participants in Phase I Trials Have Against Trial
Employers?; Luana Colloca, PhD.- Nocebo effect: The dilemma of disclosing
adverse events; Jan-Ole Reichardt, MA.- Encouraging conscientiousness in risk associated areas of medical
research Challenges in common domains of research governance; Sara Anna Suzan
Dekking, MAE et al.- Discriminating between Research and Care in Paediatric
Oncology. Ethical Appraisal of the ALL- 10 and 11 protocols of the Dutch
Childhood Oncology Group (DCOG); Imme Petersen, PhD et al.- What Does the
Child’s Assent to Research Participation Mean to Parents? Empirical Findings in
Paediatric Oncology in Germany; Marcin Waligóra, PhD.- Assent in paediatric
research and its consequences; Rosemarie Bernabe, PhD.- Ethical Issues in
Postauthorization Drug Trials; Anette Blümle, PhD et al.- Fate of Clinical
Research Studies after Ethical Approval – Follow-Up of Study Protocols until
Publication; Daniel Strech, MD, PhD.- et al. Do editorial policies support
ethical research? A thematic text analysis of author instructions in psychiatry
journals Improving common domains of research governance; Jonathan
Kimmelman, PhD.- Risk/Benefit Assessment in Launching Early Human
Trials; Annette Rid, MD.- Guidelines for Biomedical Research Involving Human Subjects
Setting Thresholds of Acceptable Research Risk: Lessons from the Debate about
Minimal Risk; Sapfo Lignou, MSc, MA et al.- Towards an Alternative Account for
Defining Acceptable Risk in Non-beneficial Pediatric Research; Roger
Brownsword, PhD.- Big biobanks: Three Major Governance Challenges and Some
Mini-Constitutional Responses; Bettina Schmietow, MA.- Dynamic Consent to
Biobank Research – Paradigm Shift or Red Herring?.

Produkt-Details

• Erscheint lt. Verlag: 9.5.2016
• Reihe/Serie: Research Ethics Forum
• Reihe/Serie: Research Ethics Forum
• Zusatzinfo: VIII, 225 p. 7 illus., 6 illus. in color.
• Verlagsort: Cham
• Sprache: englisch
• Themenwelt: Geisteswissenschaften ► Philosophie ► Allgemeines / Lexika
• Themenwelt: Medizin / Pharmazie ► Allgemeines / Lexika
• Themenwelt: Recht / Steuern
• Schlagworte: clinical research • cost-effective interventions • medical law • preclinical and clinical research • Preclinical Research • the nocebo effect
• ISBN-10: 3-319-28731-1 / 3319287311
• ISBN-13: 978-3-319-28731-7 / 9783319287317