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Regulating Medicines in Europe
Competition, Expertise and Public Health
Overview
This Book explains and investigates how medicines are controlled in Europe, especially the EU.
Research and Approach
Based on penetrating documentary and interview research with the pharmaceutical industry, regulators and consumer organisations, it provides the first major critical examination of the new Europeanised systems of medicine regulation.
Key Arguments
The authors argue that the drive to produce and approve more drugs more quickly for a single European market dominates other considerations, such as improvements in democratic accountability, the independence of regulators and scientific expertise from commercial interests, and drug safety testing and surveillance.
