Draft Human Fertilisation and Embryology (Quality and Safety) Regulations 2007; Draft Human Tissue (Quality and Safety for Human Application) Regulations 2007 PDF Download

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Draft Human Fertilisation and Embryology (Quality and Safety) Regulations 2007; Draft Human Tissue (Quality and Safety for Human Application) Regulations 2007

Author: Great Britain: Parliament: House of Commons: 1st Delegated Legislation Committee
Publisher:
ISBN: 9780215785091
Category :
Languages : en
Pages :

Book Description
Draft Human Fertilisation and Embryology (Quality and Safety) Regulations 2007; draft Human Tissue (Quality and Safety for Human Application) Regulations 2007 : Monday 21 May 2007

Human Tissue and Embryos (draft) Bill

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

Book Description
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.

Human Tissue and Embryos (Draft) Bill

Author: Great Britain: Parliament: Joint Committee on the Human Tissue and Embryos (Draft) Bill
Publisher: The Stationery Office
ISBN: 0104011432
Category : Political Science
Languages : en
Pages : 500

Book Description
The draft Bill was published in May 2007 as Command paper Cm 7087 (ISBN 9780101708722). Vol. 1 of this report is also available (ISBN 9780104011348)

Medical Treatment: Decisions and the Law

Author: Christopher Johnston
Publisher: Bloomsbury Publishing
ISBN: 1526516578
Category : Law
Languages : en
Pages : 851

Book Description
This leading textbook places medical decision-making in its legal context and provides practical guidance on the most ethically challenging cases that face the courts. It explains how the Mental Capacity Act works in practice and how the courts and lawyers wrestle with and resolve problems relating to the very essence of life: what is life? what is an acceptable quality of life? what treatment is so burdensome that it should not be attempted? These questions are posed, not in the abstract but, in real – often desperate, often urgent – situations. This is the essential guide for solicitors, barristers and judges specialising in Court of Protection work, clinical negligence, personal injury and human rights. Postgraduate medical ethics students and academics, NHS bodies and local authority professionals, health professionals and administrators in the NHS and private practice and those in Commonwealth countries with an interest in these topics will also find this book an invaluable resource. Medical Treatment: Decisions and the Law offers a readily accessible text for those dealing with the provision of medical treatment to those without capacity and related areas, providing a clear description of procedure as well as practical application of the law. Key developments for the Fourth Edition include: · The impact of the Covid-19 pandemic on decision making in the Court of Protection, particularly in relation to end of life decisions and vaccination · New chapters on two controversial issues: “the Right to Die?” and “Access to Healthcare: Choice” · Expanded chapter on Decisions for Children, covering recent high-profile cases such as Re Gard where continued provision of life sustaining treatment for babies or very young infants was at issue, and addressing the difficult issues around decision making by 16 to 17 year olds · Substantially updated chapter on Going to Court, covering how the incapacitous patient can be supported to participate in decisions about their treatment Discussion of “Escalation of Care” covering matters including NICE guidelines and care pathways and expanded coverage of issues concerning the funding of treatment. This title is included in Bloomsbury Professional's Clinical Negligence online service.

Regulating Assisted Reproductive Technologies

Author: Amel Alghrani
Publisher: Cambridge University Press
ISBN: 1107160561
Category : Health & Fitness
Languages : en
Pages : 305

Book Description
Examines emerging assisted reproductive technologies that will revolutionise the future of human reproduction and their regulation.

Stem Cell Research and the Collaborative Regulation of Innovation

Author: Sarah Devaney
Publisher: Routledge
ISBN: 1136014489
Category : Law
Languages : en
Pages : 250

Book Description
Hopes are high that stem cell (SC) research will lead to treatments and cures for some of the most serious diseases affecting humankind today. SC science has been used in a treatment setting in the replacement of patients’ windpipes and in restoring sight to patients who were blind in one eye and in future it is hoped that when the body is injured it will be able to be stimulated to produce those types of SCs necessary to repair the particular damage caused. In the meantime, research into specific treatments for a wide range of serious conditions is being undertaken including Alzheimer’s disease, cancer, and diabetes. The book considers the regulatory governance of stem cell research, setting out a readily understandable account of the science and the challenges it poses for regulators as the research is increasingly being clinically applied. It provides a critical account of those elements of a regulatory system which will be required for any jurisdiction aiming to facilitate innovative and productive SC research while maintaining appropriate ethical and legal controls. The book addresses the specific failings in the current regulatory approach to SC research in the UK and goes on to look at the regulatory approaches in the US. The book systematically analyses the roles and responsibilities of the three key participants who collaborate in this process: regulators, scientists and tissue providers, arguing that a regulatory system which fails to recognise and facilitate the vital role which each of these three groups plays runs the risk of impairing the chances of the hopes for SC research being realised. The book places a particular emphasis on ensuring that those who contribute their bodily tissues to this endeavour are treated fairly, involving a recognition that their tissues are their property.