Ethics and Governance of Biomedical Research

Theory and Practice

Daniel Strech, Marcel Mertz (Herausgeber)

Buch | Softcover

VIII, 225 Seiten

2018 | 1. Softcover reprint of the original 1st ed. 2016
Springer International Publishing (Verlag)
978-3-319-80412-5 (ISBN)

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In this book,scholars with different disciplinary and national backgrounds argue forpossible answers and analyse case studies on current issues of governance inbiomedical research. These issues comprise among others the research-caredistinction, risk evaluation in early human trials, handling of incidentalfindings, nocebo effects, cluster randomized trials, publication bias, orconsent in biobank research. This book demonstrates how new technologies andresearch possibilities multiply or intensify already known governancechallenges, leaving room for ethical analysis and complex moral choices.Clinical researchers, research ethics committee members and research ethicistshave all to deal with such challenges on a daily basis. While generalreflection on core concepts of research ethics is seldom pointless, thoseconfronted with hard moral choices do need more practical and contextualizedreflection on the said issues. This book particularly provides suchcontextualized reflectionsand aims to inform all those who study, conduct,regulate, fund, or participate in biomedical research.

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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: WhatClaims Should Healthy Participants in Phase I Trials Have Against TrialEmployers?; Luana Colloca, PhD.- Nocebo effect: The dilemma of disclosingadverse events; Jan-Ole Reichardt, MA.- Encouraging conscientiousness in risk associated areas of medicalresearch Challenges in common domains of research governance; Sara Anna SuzanDekking, MAE et al.- Discriminating between Research and Care in PaediatricOncology. Ethical Appraisal of the ALL- 10 and 11 protocols of the DutchChildhood Oncology Group (DCOG); Imme Petersen, PhD et al.- What Does theChild's Assent to Research Participation Mean to Parents? Empirical Findings inPaediatric Oncology in Germany; Marcin Waligóra, PhD.- Assent in paediatricresearch and its consequences; Rosemarie Bernabe, PhD.- Ethical Issues inPostauthorization Drug Trials; Anette Blümle, PhD et al.- Fate of ClinicalResearch Studies after Ethical Approval - Follow-Up of Study Protocols untilPublication; Daniel Strech, MD, PhD.- et al. Do editorial policies supportethical research? A thematic text analysis of author instructions in psychiatryjournals Improving common domains of research governance; JonathanKimmelman, PhD.- Risk/Benefit Assessment in Launching Early HumanTrials; Annette Rid, MD.- Guidelines for Biomedical Research Involving Human SubjectsSetting Thresholds of Acceptable Research Risk: Lessons from the Debate aboutMinimal Risk; Sapfo Lignou, MSc, MA et al.- Towards an Alternative Account forDefining Acceptable Risk in Non-beneficial Pediatric Research; RogerBrownsword, PhD.- Big biobanks: Three Major Governance Challenges and SomeMini-Constitutional Responses; Bettina Schmietow, MA.- Dynamic Consent toBiobank Research - Paradigm Shift or Red Herring?.

Erscheinungsdatum	05.03.2022
Reihe/Serie	Research Ethics Forum
Zusatzinfo	VIII, 225 p. 7 illus., 6 illus. in color.
Verlagsort	Cham
Sprache	englisch
Maße	155 x 235 mm
Gewicht	3635 g
Themenwelt	Geisteswissenschaften ► Philosophie ► Allgemeines / Lexika
	Geisteswissenschaften ► Philosophie ► Ethik
	Naturwissenschaften ► Biologie
	Recht / Steuern ► Privatrecht / Bürgerliches Recht ► Medizinrecht
Schlagworte	clinical research • cost-effective interventions • medical law • preclinical and clinical research • Preclinical Research • the nocebo effect
ISBN-10	3-319-80412-X / 331980412X
ISBN-13	978-3-319-80412-5 / 9783319804125
Zustand	Neuware