Biomedicine and Human Rights


Book Description

The Convention on Human Rights and Biomedicine, also referred to as the "Oviedo Convention", celebrated the 10th anniversary of its entry into force in 2009. This legally binding instrument aims to protect the integrity, dignity and identity of all human beings and guarantees everyone, without discrimination, the respect for their rights and fundamental freedoms with regard to the application of biology and medicine. It shares with the European Convention on Human Rights the same underlying approach and many ethical principles, and provides a general framework for the protection of fundamental rights and freedoms in the field of biomedicine. The Oviedo Convention also addresses new challenges in biomedicine that are brought about by technological and scientific developments, making it a reference text for patient rights at the European level. The principles laid down in the Oviedo Convention were further developed and complemented in additional protocols in specific fields: prohibition of cloning of human beings, transplantation of organs and tissues of human origin, and biomedical research and genetic testing for health purposes.




Additional Protocol to the Convention on Human Rights and Biomedicine, Concerning Biomedical Research


Book Description

This protocol covers the full range of research activities in the health field that involve interventions on human beings. It aims to protect the dignity and identity of everyone involved, without discrimination.




Biotechnologies and International Human Rights


Book Description

This book follows and complements the previous volume Biotechnology and International Law (Hart 2006) bringing a specific focus on human rights. It is the result of a collaborative effort which brings together the contributions of a select group of experts from academia and from international organisations with the purpose of discussing the extent to which current activities in the field of biotechnology can be regulated by existing human rights principles and standards, and what gaps, if any, need to be identified and filled with new legislative initiatives. Instruments such as the UNESCO Declaration on the Human Genome (1997) and on Bioethics and Human Rights (2005) are having an impact on customary international law. But what is the relevance of these instruments with respect to traditional concepts of state responsibility and the functioning of domestic remedies against misuse of biotechnologies? Are new legislative initiatives needed, and what are the pros and cons of a race toward the adoption of new ad hoc instruments in an area of such rapid technological development? Are there risks of normative and institutional fragmentation as a consequence of the proliferation of different regulatory regimes? Can we identify a core of human rights principles that define the boundaries of legitimate uses of biotechnology, the legal status of human genetic material, as well as the implications of the definition of the human genome as 'common heritage of humanity' for the purpose of patenting of genetic inventions? These and other questions are the focus of a fascinating collection of essays which, together, help to map this emerging field of inquiry.




Human Tissue in Transplantation and Research


Book Description

A proposal for resolving tensions between professionals and society regarding tissue for transplants and research, while properly protecting donors' interests.




The Council of Europe


Book Description

The Council of Europe, of which all European States are members, plays a pivotal role in the promotion and protection of human rights, democracy, and the rule of law in Europe. Bringing together specialist scholars and practitioners, The Council of Europe: Its Laws and Policies offers profound insights into the functioning of the organization. The organization's primary and secondary law, its institutional structure, and its far-reaching fields of activities are comprehensively and systematically analysed. This volume investigates the impact of the Council's activities within the national legal systems of the Member States and the dense web of relationships between the Council of Europe and other international organisations. An important reference work on one of the most influential organizations in Europe, the book concludes that the Council of Europe has played a considerable role in the constitutionalization process of regional public international law.







International Health Law and Ethics


Book Description

International Health Law and Ethics. Basic Documents contains a collection of treaty documents and soft law on health care rights and health ethics, used in health law training programs. Regional documents and explanatory reports on health care rights, which are derived from international human rights law, provide a way of “unwrapping” government obligations in health care, making rights more specific, accessible and (judicially) accountable. In addition, soft law declarations and medical ethics contribute to understanding the moral meaning of human rights in health care. As such, the principles and standards provide practical guidance for States when dealing with equal access to health care services, the rights of (categories of) patients, biomedical research, organ donation and transplantation, genetics and public health. These topics structure the approach of International Health Law and Ethics. This guide covers the basic documents, while general comments and explanatory reports amplify the principles embodied in the human rights treaties. The authoritative interpretations clarify a ‘European approach’ on the State’s obligations concerning health care rights and ethics. This volume is an initiative of the Erasmus Observatory on Health Law. It will be a helpful guide for all trainers, health care professionals and students interested in human rights issues in health care.




The International Law of Biotechnology


Book Description

In this thoroughly updated second edition, Matthias Herdegen provides a comprehensive and contemporary assessment of the regulation of biotechnology processes and products from an international and comparative perspective, complete with analysis of intricate legal and ethical debates.




Handbook of Forensic Medicine


Book Description

Der Goldstandard unter den Referenzwerken der Rechtsmedizin In der zweiten Auflage des Handbook of Forensic Medicine vermittelt der Herausgeber Burkhard Madea der Leserschaft einen umfassenden, internationalen Ansatz in der Rechtsmedizin mithilfe eines Teams von Experten aus aller Welt. Das Buch enthält neue Inhalte zu den Themen Tatortuntersuchung, Analyse von Blutfleckenmustern, Terroranschläge, Brandkatastrophen, neue psychoaktive Substanzen und Molekularpathologie sowie einen umfassenden Überblick über sämtliche Aspekte der Rechtsmedizin. In den einzelnen Kapiteln werden alle Faktoren der Qualitätskontrolle und Best Practices behandelt. Anhand von Fallstudien werden die dort erläuterten Konzepte veranschaulicht und die Verbindungen zwischen verschiedenen Teildisziplinen hervorgehoben. Für Spezialisten, die täglich im Einsatz sind, werden in jedem Kapitel die Elemente der Routineanalyse behandelt. In der zweiten Auflage des Handbook of Forensic Medicine werden die neuesten Entwicklungen in der forensischen Molekularbiologie, der forensischen Toxikologie, der Molekularpathologie und der Immunhistochemie besprochen. Darüber hinaus bietet das Werk: * Eine gründliche Einführung in die Aufgaben der Rechtsmedizin in der modernen Gesellschaft mit einer Darstellung der internationalen Richtlinien und Akkreditierungen in der Rechtsmedizin * Umfassende Betrachtungen der medizinischen Aspekte des Todes, insbesondere des Wesens und der Definition von Tod, Autopsie und der Identifizierung der Opfer von Massenkatastrophen * Praktische Erörterungen zur Traumatologie und zum gewaltsamen Tod, insbesondere durch Ersticken, Stromschlag und Blitzschlag, Kindstötung und ärztliche Kunstfehler * Tiefgreifende Untersuchungen zum plötzlichen und unerwarteten Tod aus natürlichen Gründen, auch zur Biochemie nach dem Tod Dieses Buch ist unverzichtbar für jeden Experten in der Rechtsmedizin, Toxikologie und Hämogenetik sowie für alle, die Gutachten für Gerichtsverfahren erstellen sollen. Auch für Rechtsanwälte und Jurastudenten ist es ein ideales Nachschlagewerk.