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Author: World Health Organization
Publisher: World Health Organization
ISBN: 9241564040
Category : Medical
Languages : en
Pages : 147
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Book Description
Background papers 1 to 9 published as technical documents. Available in separate records from WHO/HSS/EHT/DIM/10.1 to WHO/HSS/EHT/DIM/10.9
Author: World Health Organization
Publisher: World Health Organization
ISBN: 9241564040
Category : Medical
Languages : en
Pages : 147
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Book Description
Background papers 1 to 9 published as technical documents. Available in separate records from WHO/HSS/EHT/DIM/10.1 to WHO/HSS/EHT/DIM/10.9
Author: IBP, Inc.
Publisher: Lulu.com
ISBN: 1433069423
Category : Business & Economics
Languages : en
Pages : 304
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Book Description
Four interlocking narratives unfurl in four American cities, creating a richly comic feast about love, academia, an elusive Tibetan novelist who might be a plagiarist, and SOFA, a protest group so mysterious its very initials are open to interpretation. Bad Teeth follows a cast of young literary men and women in four very American cities—Brooklyn, Bloomington, Berkeley, and Bakersfield. It’s four (or more) books in one, a Pynchonesque treat: a bohemian satire, a campus comedy, a stoner’s reverie, and a quadruple love story. Its wonderfully evoked storylines of young writers—each in a period of formation—collect around the search for one mysterious author—"the Tibetan David Foster Wallace," who might in fact be a plagiarist.This delightful and complex literary novel is a comic gem.
Author: Paul Craig
Publisher: Oxford University Press, USA
ISBN: 0199576998
Category : Law
Languages : en
Pages : 1317
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Book Description
The fifth edition of EU Law: Text, Cases, and Materials provides clear and insightful analysis of European Law accompanied by carefully chosen extracts from a range of materials. This edition looks in detail at the way in which the Treaty of Lisbon has radically changed both the institutional and substantive law of the European Union.
Author: Christa Altenstetter
Publisher: Routledge
ISBN: 1351506285
Category : Medical
Languages : en
Pages : 277
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Book Description
Medical devices are the bread and butter from which health care and clinical research are derived. Such devices are used for patient care, genetic testing, clinical trials, and experimental clinical investigations. Without medical devices, there is no clinical research or patient care. Without life-adjusting devices, there are no medical procedures or surgery. Without life-saving and life-maintaining devices, there is no improvement in well-being and quality of life. Without innovative medical devices and experimentation, there can be no medical progress or patient safety. Medical devices and medical technology are used to create or support many different products and medical-surgical procedures. This volume on the regulation of medical devices in the European Union, with a focus on France, tackles a topic of interdisciplinary interest and significance for policymakers in countries around the globe. The EU regulatory regime is one of three global regional regimes, and medical products manufactured in EU countries are sold worldwide. As countries confront an aging population on a global scale, with associated increases in chronic diseases, physical handicaps, and multi-morbidity, there will inevitably be an increase in the demand for health services and, concomitantly, the use of medical devices in medical and surgical procedures. This will be the case regardless of whether services are delivered in hospitals, doctors' offices, or at home. The associated risks of a particular device will be the same whatever the country of origin for the device, or where the need occurs. Revolutionary medical advances increase diagnostic capabilities, but they increase the potential of harm and risks to patients. Medical technologies and devices are used ethically most of the time; yet they have the potential for unethical use when scientific medicine is elevated over human life and death. Assumptions that are taken for granted can be dangerous to a patient's health. That is why our understanding of appropriate and effective regulation of medical devices is significant to all people on all continents.
Author:
Publisher:
ISBN:
Category : International law
Languages : en
Pages : 280
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Book Description
Author: Naval War College (U.S.)
Publisher:
ISBN:
Category : War (International law)
Languages : en
Pages : 256
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Book Description
Author:
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 1260
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Book Description
Author: Christian Baumgartner
Publisher: Springer Nature
ISBN: 3031220919
Category : Technology & Engineering
Languages : en
Pages : 671
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Book Description
This updatable reference work gives a comprehensive overview of all relevant regulatory information and requirements for manufacturers and distributors around medical and in-vitro diagnostic devices in Europe. These individual requirements are presented in a practice-oriented manner, providing the reader with a concrete guide to implementation with main focus on the EU medical device regulations, such as MDR 2017/745 and IVD-R 2017/746, and the relevant standards, such as the ISO 13485, ISO 14971, among others. This book offers a good balance of expert knowledge, empirical values and practice-proven methods. Not only it provides readers with a quick overview about the most important requirements in the medical device sector, yet it shows concrete and proven ways in which these requirements can be implemented in practice. It addresses medical manufacturing companies, professionals in development, production, and quality assurance departments, and technical and medical students who are preparing themselves for a professional career in the medical technlogy industries.
Author: New York (State). Legislature
Publisher:
ISBN:
Category : New York (State)
Languages : en
Pages : 756
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Author:
Publisher:
ISBN:
Category : Austria
Languages : en
Pages : 566
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Book Description
