Law and the Regulation of Medicines
មីនា 2012 · Bloomsbury Publishing
2.9star
ការវាយតម្លៃ 8
សៀវភៅអេឡិចត្រូនិច
308
ទំព័រ
អំពីសៀវភៅអេឡិចត្រូនិកនេះ
The principal purpose of this book is to tell the story of a medicine's journey through the regulatory system in the UK, from defining what counts as a medicine, through clinical trials, licensing, pharmacovigilance, marketing and funding. The question of global access to medicines is addressed because of its political importance, and because it offers a particularly stark illustration of the consequences of classifying medicines as a private rather than a public good.
Two further specific challenges to the future of medicine's regulation are examined separately: first, pharmacogenetics, or the genetic targeting of medicines to subgroups of patients, and second, the possibility of using medicines to enhance well-being or performance, rather than treat disease.
Throughout, the emphasis is on the role of regulation in shaping and influencing the operation of the medicines industry, an issue that is of central importance to the promotion of public health and the fair and equitable distribution of healthcare resources.
Two further specific challenges to the future of medicine's regulation are examined separately: first, pharmacogenetics, or the genetic targeting of medicines to subgroups of patients, and second, the possibility of using medicines to enhance well-being or performance, rather than treat disease.
Throughout, the emphasis is on the role of regulation in shaping and influencing the operation of the medicines industry, an issue that is of central importance to the promotion of public health and the fair and equitable distribution of healthcare resources.
ការដាក់ផ្កាយ និងមតិវាយតម្លៃ
2.9
ការវាយតម្លៃ 8
អំពីអ្នកនិពន្ធ
Emily Jackson is Professor of Law at the London School of Economics.
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