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  1. Variations and voids: the regulation of human cloning around the world. [REVIEW]Shaun D. Pattinson & Timothy Caulfield - 2004 - BMC Medical Ethics 5 (1):1-8.
    Background No two countries have adopted identical regulatory measures on cloning. Understanding the complexity of these regulatory variations is essential. It highlights the challenges associated with the regulation of a controversial and rapidly evolving area of science and sheds light on a regulatory framework that can accommodate this reality. Methods Using the most reliable information available, we have performed a survey of the regulatory position of thirty countries around the world regarding the creation and use of cloned embryos (see Table (...)
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  • Participation of Children in Medical Decision-Making: Challenges and Potential Solutions.Vida Jeremic, Karine Sénécal, Pascal Borry, Davit Chokoshvili & Danya F. Vears - 2016 - Journal of Bioethical Inquiry 13 (4):525-534.
    Participation in healthcare decision-making is considered to be an important right of minors, and is highlighted in both international legislation and public policies. However, despite the legal recognition of children’s rights to participation, and also the benefits that children experience by their involvement, there is evidence that legislation is not always translated into healthcare practice. There are a number of factors that may impact on the ability of the child to be involved in decisions regarding their medical care. Some of (...)
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  • Research site monitoring for compliance with ethics regulatory standards: review of experience from Uganda. [REVIEW]Joseph Ochieng, Julius Ecuru, Frederick Nakwagala & Paul Kutyabami - 2013 - BMC Medical Ethics 14 (1):23.
    On site monitoring of research is one of the most effective ways to ensure compliance during research conduct. However, it is least carried out primarily for two reasons: presumed high costs both in terms of human resources and finances; and the lack of a clear framework for undertaking site monitoring. In this paper we discuss a model for research site monitoring that may be cost effective and feasible in low resource settings.
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  • Variations and voids: the regulation of human cloning around the world.Caulfield Timothy & D. Pattinson Shaun - 2004 - BMC Medical Ethics 5 (1):9.
    Background No two countries have adopted identical regulatory measures on cloning. Understanding the complexity of these regulatory variations is essential. It highlights the challenges associated with the regulation of a controversial and rapidly evolving area of science and sheds light on a regulatory framework that can accommodate this reality. Methods Using the most reliable information available, we have performed a survey of the regulatory position of thirty countries around the world regarding the creation and use of cloned embryos. We have (...)
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  • The New Belgian Law on Biobanks: Some Comments from an Ethical Perspective.Sigrid Sterckx & Kristof Van Assche - 2011 - Health Care Analysis 19 (3):247-258.
    On 19 December 2008 the Official Journal of Belgium published the ‘Law regarding the procurement and use of human body material destined for human medical applications or for scientific research purposes’. This paper will comment on various aspects of the Law: its scope of application (what is understood by ‘body material’?); its concept of ‘residual human body material’ (with far-reaching implications for the type of consent required for research); the nature of actions with and uses of human body material that (...)
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  • Medical research in clinical emergency settings in Europe.S. Lötjönen - 2002 - Journal of Medical Ethics 28 (3):183-187.
    Clinical emergencies necessitate immediate action to avert the danger to the patient's life or health. Emergency patients might be in greatest need of novel therapies, and even presumed willing to assume some risk, but research into emergency conditions should be conducted under commonly accepted principles that fulfil the scientific, ethical, and legal criteria. Such criteria already exist in the US, but are still under development in Europe.This article introduces criteria upon which trials in emergency settings may be ethically and legally (...)
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  • Classical Distributive Justice and the European Healthcare System: Rethinking the Foundations of European Health Care in an Age of Crises.Stéphane Bauzon - 2015 - Journal of Medicine and Philosophy 40 (2):190-200.
    The state subvention and distribution of health care not only jeopardize the financial sustainability of the state, but also restrict without a conclusive rational basis the freedom of patients to decide how much health care and of what quality is worth what price. The dominant biopolitics of European health care supports a healthcare monopoly in the hands of the state and the medical profession, which health care should be opened to the patient’s authority to deal directly for better basic health (...)
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