Affiliations: Max-Weber-Institute for Sociology, University of
Heidelberg, Bergheimer Straße 58, 69115 Heidelberg, Germany. Tel.: +49
6221542995; E-mail: [email protected]
Abstract: After more then four decades, the regulation of pharmaceuticals
still is an evolving and much discussed topic within Europe from a political
and economic perspective. Even though the benefits of regulatory harmonization
remain uncontested, the constant review and evaluation of the sector may raise
public concerns regarding regulatory performance. If regulatory 0experts still
see the need for improving existing regulatory provisions, there is reason to
believe that the current system does not live up to its expectations. An
assessment of regulatory effectiveness, depicting the degree of goal
attainment, provides a systematic answer to such questions. Drawing on the
regulatory framework, the governance and the outcomes of the regulatory process
the development of regulatory effectiveness since the beginnings of European
regulation in the sector is discussed. While a continuous improvement from the
perspective of effectiveness is traceable throughout time, some issues impeding
the performance of the regulatory regime remain. Even though the pharmaceutical
package may help to mitigate some of the identified problems, additional
efforts will be necessary to finally strengthen the effectiveness of European
pharmaceutical regulation and public health.
Keywords: European pharmaceutical policy, regulatory quality, effectiveness of regulation