Human Fertilisation and Embryology (disclosure of Information) [H.L.] A Bill Intituled an Act to Relax the Restrictions on the Disclosure of Information Imposed by Section 33(5) of the Human Fertilisation and Embryology Act 1990 PDF Download

Author: Great Britain. Parliament. House of Commons
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Author: Great Britain. Parliament. House of Commons
Publisher:
ISBN: 9780103050935
Category : Artificial insemination, Human
Languages : en
Pages : 3

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Author: Great Britain: Department of Health
Publisher: The Stationery Office
ISBN: 9780101708722
Category : Medical
Languages : en
Pages : 250

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The Government set out detailed policy proposals for changes to the Human Fertilisation and Embryology Act 1990 in its White Paper (Cm.6989, ISBN 9780101698924) published in December 2006. These proposed changes to the law and regulation relating to human reproductive technologies, following on from a public consultation exercise undertaken during 2005, sought to balance the competing claims of reproductive liberty and responsibility, patient safety, child welfare, professional autonomy and public accountability. The overarching aim is to achieve the common good through a system which is broadly acceptable to society, given the complex ethical issues involved, and which is effective given the pace of scientific developments. This present document contains the draft text of the proposed Human Tissue and Embryos Bill, published in order to enable pre-legislative scrutiny of the proposals by a Parliamentary Committee. It includes the text of the draft Bill, explanatory notes, a draft regulatory impact assessment and a version of how the Human Fertilisation and Embryology Act would look if amended by the draft Bill and the EU Tissue Directive. The proposals include the creation of the new single regulatory authority on the use of human tissue, cells and blood, to be called the Regulatory Authority for Tissue and Embryos (RATE), to replace the Human Fertilisation and Embryology Authority and the Human Tissue Authority.

Author: Great Britain
Publisher:
ISBN: 9780111497692
Category : Law
Languages : en
Pages : 12

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Enabling power: Human Fertilisation and Embryology Act 1990, ss. 33D, 45 (1) to (3A). Issued: 30.03.2010. Made: 24.03.2010. Laid: -. Coming into force: 06.04.2010. Effect: None. Territorial extent & classification: E/W/S/NI. General. Supersedes draft S.I. (ISBN 9780111491256) issued 26.01.2010

Author: Great Britain
Publisher:
ISBN: 9780110493992
Category : Law
Languages : en
Pages : 4

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Enabling power: Human Fertilisation and Embryology Act 1990, ss. 31 (4) (a), 45 (1) to (3). Issued: 22.06.2004. Made: 14.06.2004. Laid: -. Coming into force: 01.07.2004. Effect: None. Territorial extent & classification: E. General

Author:
Publisher:
ISBN: 9781904384106
Category : Animal experimentation
Languages : en
Pages : 335

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A report of the Nuffield Council on Bioethics working party investigating the ethical issues of research involving animals.

Author:
Publisher:
ISBN:
Category : Health promotion
Languages : en
Pages : 336

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Author: Reva B. Siegel
Publisher:
ISBN: 9780615648217
Category : Abortion
Languages : en
Pages : 390

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"As the landmark Roe v. Wade decision reaches its 40th anniversary, abortion remains a polarizing topic on America's legal and political landscape. Blending history, culture, and law, Before Roe v. Wade eplores the roots of the conflict, recovering through original documents and first-hand accounts the voices on both sides that helped shape the climate in which the Supreme Court ruled. Originally published in 2010, this new edition includes a new Afterword that explores what the history of conflict before Roe teaches us about the abortion conflict we live with today. Examining the role of social movements and political parties, the authors cast new light on a pivotal chapter in American history and suggest how Roe v. Wade, the case, because Roe v. Wade, the symbol. "--Cover, p. 4.

Author: Michael Wells-Greco
Publisher:
ISBN: 9789462366121
Category : Adopted children
Languages : en
Pages : 0

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Through a comparative review of eight legal systems, this book examines the legal aspects of parenthood and nationality following inter-country surrogacy arrangements and the influence of European and international human rights law on the determination of parentage, the establishment of nationality, and the prevention of statelessness, as well as identity rights, continuation of relationship rights, and, more broadly, child protection. The research considers whether national laws on parenthood and the establishment of nationality sufficiently protect the interests of the surrogate-born child, as well as the parties to a surrogacy arrangement in accordance with identifiable standards under European and international human rights law. Soft law and hard law recommendations are provided to protect the interests of these children. Thesis. *** Librarians: ebook available [Subject: International Law, European Law, Human Rights Law, Family Law, Children's Law, Comparative Law]

Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 030929665X
Category : Medical
Languages : en
Pages : 78

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Gene transfer research is a rapidly advancing field that involves the introduction of a genetic sequence into a human subject for research or diagnostic purposes. Clinical gene transfer trials are subject to regulation by the U.S. Food and Drug Administration (FDA) at the federal level and to oversight by institutional review boards (IRBs) and institutional biosafety committees (IBCs) at the local level before human subjects can be enrolled. In addition, at present all researchers and institutions funded by the National Institutes of Health (NIH) are required by NIH guidelines to submit human gene transfer protocols for advisory review by the NIH Recombinant DNA Advisory Committee (RAC). Some protocols are then selected for individual review and public discussion. Oversight and Review of Clinical Gene Transfer Protocols provides an assessment of the state of existing gene transfer science and the current regulatory and policy context under which research is investigated. This report assesses whether the current oversight of individual gene transfer protocols by the RAC continues to be necessary and offers recommendations concerning the criteria the NIH should employ to determine whether individual protocols should receive public review. The focus of this report is on the standards the RAC and NIH should use in exercising its oversight function. Oversight and Review of Clinical Gene Transfer Protocols will assist not only the RAC, but also research institutions and the general public with respect to utilizing and improving existing oversight processes.