Medicinal Product Liability and Regulation, Richard Goldberg
Автор: Tulibacka Название: Product Liability Law in Transition ISBN: 1138262528 ISBN-13(EAN): 9781138262522 Издательство: Taylor&Francis Рейтинг: Цена: 53070.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: This volume examines the evolution of Central European product liability regimes, with particular reference to the effect of the implementation of the Product Liability Directive in the context of the recent enlargement of the EU.
Автор: Krapohl, Sebastian Название: Risk regulation in the single market ISBN: 0230537650 ISBN-13(EAN): 9780230537651 Издательство: Springer Рейтинг: Цена: 83850.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: This book demonstrates how the Thalidomide catastrophe of the 1960s and the BSE crisis of the 1990s led to regulatory regimes for pharmaceuticals and foodstuffs in Europe. However, the developmental paths of these regimes differ - and so does the efficiency and legitimacy of regulatory policy-making.
Автор: Liedtke Название: The Future of Insurance Regulation and Supervision ISBN: 0230292690 ISBN-13(EAN): 9780230292697 Издательство: Springer Рейтинг: Цена: 139750.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: Written by leading academics, researchers and insurance industry experts, this book offers a diversified perspective on how the regulatory and supervisory framework for the insurance sector will develop over the coming years. It is supported by The Geneva Association , the world-leading insurance think-tank of the private industry.
Автор: Davis Название: Unhealthy Pharmaceutical Regulation ISBN: 0230008666 ISBN-13(EAN): 9780230008663 Издательство: Springer Рейтинг: Цена: 130610.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: This is the first book to examine how effectively American and supranational EU governments have regulated innovative pharmaceuticals during the last 30 years regarding public health. It explains why pharmaceutical regulation has been misdirected by commercial interests and misconceived ideologies.
Автор: Golombok Название: Regulating Reproductive Donation ISBN: 1107090962 ISBN-13(EAN): 9781107090965 Издательство: Cambridge Academ Рейтинг: Цена: 81310.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: The emergence of new empirical evidence and ethical debate has called into question the current regulatory frameworks that govern reproductive donation, both in the UK and overseas. In response, this book offers fresh interdisciplinary perspectives on current challenges facing the regulation of reproductive donation, and suggests possible ways forward.
Автор: Calvo Caravaca Название: The EU Succession Regulation ISBN: 1107127300 ISBN-13(EAN): 9781107127302 Издательство: Cambridge Academ Рейтинг: Цена: 172130.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: Written by leading experts in the field, this book offers a detailed article-by-article analysis of the European Succession Regulation. It provides an authoritative guide to judges, notaries, holders of public records and lawyers in private practice.
Автор: Waldemar Wojcik Название: Information Technology in Medical Diagnostics ISBN: 1138299294 ISBN-13(EAN): 9781138299290 Издательство: Taylor&Francis Рейтинг: Цена: 132710.00 T Наличие на складе: Невозможна поставка. Описание:
For many centuries, people have tried to learn about the state of their health. Initially, in the pre-technological period, they had to rely only on their senses. Then there were simple tools to help the human senses. The discovery of X-rays, which allowed people to look "inside" the body, turned out to be a major breakthrough. Contemporary medical diagnostics is increasingly being assisted by information technology that allows, for example, thorough image tissue analysis or pathology differentiation. They also allow very early preventive diagnostics. Influenced by information technology, "classic" diagnostic techniques change and new ones arise.
Information Technology in Medical Diagnostics presents selected and extended conference papers from Polish, Ukrainian and Kazakh scientists. They address problems of the application of new methods of image processing for analysis of medical images, new methods of classification of medical data as well as new medical imaging methods. Some of the presented technologies are inspired by the functioning of living organisms.
Information Technology in Medical Diagnostics is of interest not only to academics and engineers, but also to professionals involved in biomedical engineering, and seeking for solutions for issues that cannot be solved with the help of "traditional" technologies.
Автор: Dieter D?rr, Russell L. Weaver Название: Perspectives on Privacy: Increasing Regulation in the USA, Canada, Australia and European Countries ISBN: 3110338173 ISBN-13(EAN): 9783110338171 Издательство: Walter de Gruyter Цена: 99110.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: Due to rapid developments in the communication sector, the right to privacy faces new challenges. The increasing digitization and internationalization of communication processes have raised a number of issues, and lead to conflicts wherever national legal systems and moral concepts collide. Particularly in the areas of data protection and liability of online service providers, universal approaches are required. This title presents positions of specialists in Europe, Australia, the US and Canada which contribute to the international dialogue and thereby offer a starting point for a sustainable policy for the protection of privacy rights
Автор: Matthew W Hill, Daniel E Torres Название: FDA Oversight of Medical Devices: Efforts & Developments ISBN: 1622570898 ISBN-13(EAN): 9781622570898 Издательство: Nova Science Рейтинг: Цена: 168950.00 T Наличие на складе: Невозможна поставка. Описание: The FDA is responsible for overseeing the safety and effectiveness of medical devices sold in the United States. New devices are generally subject to FDA review via the 510(k) process, which determines if a device is substantially equivalent to another legally marketed device, or the more stringent pre-market approval process, which requires evidence providing reasonable assurance that the device is safe and effective. This book examines whether the FDA is sufficiently meeting the performance goals and whether devices are reaching the market in a timely manner.
Название: Progress in Ensuring Adequate Access to Internationally Controlled Substances for Medical and Scientific Purposes: Supplement to the Report of the Board for 2018 ISBN: 9211483107 ISBN-13(EAN): 9789211483109 Издательство: Mare Nostrum (Eurospan) Рейтинг: Цена: 21250.00 T Наличие на складе: Поставка под заказ. Описание: The preamble of the Single Convention of 1961 highlights the concern of States for the health and welfare of humankind. This assertion is followed by the recognition of the medical use of narcotic drugs and their indispensable role in the relief of pain for which countries needed to ensure the availability and to make adequate provision.
Автор: Franco Ferrari Название: Concise Commentary on the Rome I Regulation ISBN: 1108497675 ISBN-13(EAN): 9781108497671 Издательство: Cambridge Academ Рейтинг: Цена: 158400.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: Authored by an international group of scholars, this book focuses on the most relevant instrument used throughout Europe to determine what law applies to international contracts. It will appeal to practitioners and scholars looking to explore the Rome I Regulation.
Автор: Cohen, I. Glenn Название: Future of medical device regulation ISBN: 1108972055 ISBN-13(EAN): 9781108972055 Издательство: Cambridge Academ Рейтинг: Цена: 36950.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание: As the nature of medical devices is rapidly changing, the legal and ethical questions around medical devices are becoming ever more complex. This volume analyses the current issues and controversies around patient privacy, innovation, and new regulatory laws in the US and EU.
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