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Law and the regulation of medicines /

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 add...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Jackson, Emily, 1966-
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Oxford ; Portland, Ore. : Hart Pub., 2012.
Temas:
Acceso en línea:Texto completo

MARC

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245 1 0 |a Law and the regulation of medicines /  |c Emily Jackson. 
260 |a Oxford ;  |a Portland, Ore. :  |b Hart Pub.,  |c 2012. 
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505 0 |a What are medicines and why are they special? -- Clinical trials -- Licensing -- Pharmacovigilance and liability for dangerous drugs -- Marketing -- Funding and access to medicines in the UK -- Funding and access to medicines : a global problem -- The future of medicines I : pharmacogenetics -- The future of medicines II : enhancement. 
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520 |a 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. 
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