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We study the effects of a change in the way patient reimbursements are calculated on the prices of pharmaceuticals using quasi-experimental data for Denmark which switched from external (where reimbursements are based on prices of similar products in foreign countries) to internal reference...
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We examine how the U.S. Food and Drug Administration Amendments Act (FDAAA) of 2007, which requires additional disclosures regarding clinical trial results, impacts information asymmetry between the disclosing pharmaceutical firm and capital market participants, the general public, academics,...
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treaties is untenable and risks undermining basic principles of international law. States enacting cannabis regulation must … drug control conventions so as to accommodate cannabis regulation is not feasible for the foreseeable future, and the … regulation with arguments of citizens’ health and safety, and justifying it with an appeal to human rights obligations; (4 …
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also characterized by extensive regulation of almost every activity, from product development through manufacturing and …
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