Titlebook: Human Medical Research; Ethical, Legal and S Jan Schildmann,Verena Sandow,Jochen Vollmann Book 2012 Springer Basel AG 2012 Clinical researc

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Biomedical Research in Developing Countries and International Human Rights Lawcipate in a single project. Furthermore, internationally-based organizations may be able to choose the country in which a particular research project that they are conducting or funding is carried out. This has led to concerns being expressed about the possibility of fundamentally different standard

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Conflicts of Interest in Medical Research: What can Ethics Contribute?r vaguely defined. In addition, the ethical foundations of the current demand for strategies to manage conflicts of interest are rarely made explicit. The aim of this paper is to clarify the concept of conflicts of interest and to analyse the underlying ethical principles. In a first step, we analys

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Research Ethics in Genomics Research: Feedback of Individual Genetic Data to Research Participantste has rapidly gained in urgency in view of the emergence of biobanks and the advances in next-generation sequencing technology, which has the potential to generate unequalled amounts of genetic data. This implies that the generation of many known and unknown genetic variants in individual participa

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Regulating “Higher Risk, No Direct Benefit” Studies with Children: Challenging the US Federal Regulaatients for each proposed medical research study. If the study involves children and cannot directly benefit those children, the risks and burdens involved cannot be more than “minimal”. The two relevant ethics documents recognized in Europe forbid review boards to make any exceptions to the require

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A Paradigm Change in Research Ethicsd mainly on negative obligations towards human subjects, such as the idea that participants must not be exploited or not be used merely as a means. A theory of research ethics should also take into account the positive obligations of what we owe to human beings. However, in order to establish this t

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