The Collection and Use of Human Blood and Plasma in the Non-European Union Council of Europe Member States in 1995 PDF Download
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Author: A. Rejman
Publisher: Council of Europe
ISBN: 9789287133588
Category : Political Science
Languages : en
Pages : 118
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Book Description
Author: A. Rejman
Publisher: Council of Europe
ISBN: 9789287133588
Category : Political Science
Languages : en
Pages : 118
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Book Description
Author: Council of Europe
Publisher: Council of Europe
ISBN: 9789287153937
Category : Medical
Languages : en
Pages : 266
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Book Description
Author: Council of Europe
Publisher: Council of Europe
ISBN: 9789287145604
Category : Medical
Languages : en
Pages : 84
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Book Description
Methods aimed at inactivation of pathogens in labile blood products have been developed in recent years. Their use raises a number of issues, including efficiency, the damage inflicted to the blood products, the toxicity for patients, and the cost-benefit ratio. In the foreseeable future, national blood transfusion services and health authorities will have to consider the introduction of these methods. The report summarises the current information on these pathogen inactivation procedures.
Author: Council of Europe
Publisher: Council of Europe
ISBN: 9789287136329
Category : Political Science
Languages : en
Pages : 100
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Book Description
Author: Bernard Genetet
Publisher: Council of Europe
ISBN: 9789287137166
Category : Political Science
Languages : en
Pages : 68
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Book Description
Author: José Luis Valverde
Publisher: IOS Press
ISBN: 9781586035211
Category : Business & Economics
Languages : en
Pages : 154
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Book Description
In the domain of public policy on pharmaceuticals, protecting public health requires a dual strategy: robust regulation on the one hand and stimulation of competitiveness and innovation on the other. Regulation must be robust to ensure that only medicines meeting exact standards of safety, quality and efficacy are authorised for human and animal use. At the same time competitiveness and innovation must be stimulated. Without innovation in pharmaceuticals, the incurable diseases of today will remain incurable. Competitiveness drives innovation and innovation saves lives. Increased competitiveness of the pharmaceutical sector will not only better protect public health, but will also create high quality jobs and create growth. In this context the implementation of the G10 recommendations, particularly regarding the pricing and reimbursement of medicines by Member States, remains a considerable challenge.
Author: Council of Europe
Publisher: Manhattan Publishing Company
ISBN:
Category : Medical
Languages : en
Pages : 184
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Book Description
Author: Tamara K. Hervey
Publisher: Cambridge University Press
ISBN: 1107010497
Category : Law
Languages : en
Pages : 749
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Book Description
The first holistic and thematic study of EU health law, and its implications, through its own internal logics.
Author: Anne-Maree Farrell
Publisher: Cambridge University Press
ISBN: 110737569X
Category : Law
Languages : en
Pages : 283
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Book Description
How best to manage risk involving multi-valued human biological materials is the overarching theme of this book, which draws on the sourcing and supply of blood as a case study. Blood has ethical, social, scientific and commercial value. This multi-valuing process presents challenges in terms of managing risk, therefore making it ultimately a matter for political responsibility. This is highlighted through an examination of the circumstances that led to HIV blood contamination episodes in the US, England and France, as well as their consequences. The roles of scientific expertise and innovation in managing risks to the blood system are also analysed, as is the increased use of precautionary and legal strategies in the post-HIV blood contamination era. Finally, consideration is given to a range of policy and legal strategies that should underpin effective risk governance involving multi-valued human biological materials.
Author: Tamara K. Hervey
Publisher: Cambridge University Press
ISBN: 1139455354
Category : Law
Languages : en
Pages : 541
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Book Description
How does the law of the European Union affect health law and policy? At first sight, it seems limited. However, despite its restricted formal competence, the EU has recently become increasingly involved in the health field. Litigation based on EU law has resulted in a 'right to receive health care services' across national boundaries which may have huge practical implications for national health systems. The EU has promulgated legislation regulating clinical research, and the marketing of pharmaceuticals; patients' rights are affected by EU legislation on data protection and product liability; the qualifications of health care professionals are legally recognised across the EU; and the EU has acted to promote public health. This book explores the various impacts of measures of EU law on national health law and policy. Through elaboration of selected examples, the authors show that, within the EU, health law cannot be regarded as a purely national affair.
