Titlebook: Regulation of the Pharmaceutical Industry; John Abraham (Professor of Sociology and Co-direct Book 2003 Palgrave Macmillan, a division of

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Europeanization of Medicines Regulation, the relevant EU organizations, conducted between 1994 and 1998. In particular we focus on the politics of scientific expertise within the Europeanization process and the implications of the latter for drug safety, public health and the democratic accountability of regulatory decision making.

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Sales Licensing Documentation and Trade Secrecy: the case of NorplantR Contraceptives,ortant form of public regulation on drugs. Based on the information provided by the product license holder, the drug regulatory authorities evaluate the risks and benefits of the drug during the sales licensing process to determine whether the drug should be allowed to enter the markets of that country.

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2947-3829 be determined by scientific experts, a democratic state, the interests of final users, or ethical principles? This unique collection brings together the work of social scientists, ethicists, lawyers and policy analysts on regulation, ethics and innovation in the pharmaceutical industry. Regulatory s

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The Limitations of Current Ethical Regulations,ncipatory status. I draw upon a number of studies to illustrate the effects of the implementation of informed consent in various social contexts. Finally, I argue the central role accorded to informed consent obfuscates other ethical issues relating to the broader political and institutional setting

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Introduction,rmaceutical industry’ and ‘regulation’. This is not entirely straightforward because regulation shapes the industry and vice-versa. In some contexts, technological innovations may drive the construction of regulations and governance. For this reason it is important to examine the process of pharmace

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