In recent years the need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not only lawyers but also hospitals, researchers, prescribers and many others involved in the provision of healthcare. Such a need has been precipitated by a number of factors including the changing structure of healthcare in the UK and Europe, the increasing specialisation in litigation relating to medicines' control and provision and the various changes in regulation that have arisen both from challenges in the courts and from the intervention of public bodies. Until now the information resources available to those involved in the complex interrelations between medicines, medical devices and the law have remained scarce. This book is designed to address this situation by bringing together the knowledge of the laws governing the regulation of medicines of the most experienced and qualified experts in one volume ranging across all aspects of the field. All areas of the law relating to the research, development, manufacture, distribution and dispensation of medicines and medical devices in the UK are covered as well as various topics within the law governing responsibilities, procedures and compensation in cases of malpractice and injury.
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This book provides specialist knowledge regarding the regulation of medicines. It collates information of the laws governing regulation from the most experienced and qualified experts, and does so in one volume covering all aspects of the field. All areas of the law relating to the research, development, manufacture, distribution and dispensation of medicines and medical devices in the UK are covered as well as various topics within the law governing responsibilities, procedures and compensation in cases of malpractice and injury.
"This is a book that has been needed for the last decade. The need has been filled with this excellent book written and edited by people who are highly competent in their specialist fields. For those who had not realized that they needed this book it should, perhaps, be spelt out clearly who should have a copy on their shelves - pharmaceutical physicians, registration managers, pharmaceutical company lawyers, lawyers practising in the field of medical malpractice and negligence and managers of National Health Service (NHS) trusts." - Reviewed by J P Griffin Review published in Adverse Drug Reactions and Toxicological Reviews Volume 19, Number 1, 2000
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Paperback. Condition: new. Paperback. The need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not only lawyers but also hospitals, researchers, prescribers and many others involved in the provision of healthcare. Such a need has been precipitated by a number of factors, including the changing structure of healthcare in the UK and Europe and the various changes in regulation that have arisen both from challenges in the courts and from the intervention of public bodies. However, the information available to those involved in the complex interrelations between medicines, medical devices and the law have remained scarce. This book aims to address this situation by bringing together the knowledge of the laws governing the regulation of medicines ranging across the field from the ethics of the use of medicines in treatment and research, through to drug-induced injury, civil liability and no-fault compensation schemes. This book aims to address the lack of information available to those involved in the complex interrelations between medicines, medical devices and the law by bringing together the knowledge of the laws governing the regulation of medicines, ranging across the field. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Seller Inventory # 9780521292511
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