In the domain of public policy on pharmaceuticals, protecting public health requires a dual strategy: robust regulation on the one hand and stimulation of compe
This book provides an analysis of European Union pharmaceutical regulation from a policy-making perspective. The focus is on how the often conflicting agendas o
This book analyses the implementation of global pharmaceutical impact standards in the European risk regulation framework for pharmaceuticals and questions its
Fully revised and updated, this practical book contains information on the processes, legislation, cases and customs that apply to the introduction, marketing a
Globalization is rapidly changing lives and industries around the world. Drug development, authorization, and regulatory supervision have become international e