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EC Pharmaceutical Law

(Autor)

Loseblattwerk
400 Seiten
1992
Chancery Law Publishing (Verlag)
978-0-471-93648-0 (ISBN)
CHF 589,95 inkl. MwSt
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A manual which is designed to provide better understanding of the EC pharmaceutical law. The first section of the book presents the legislation, and the second section gives detailed commentary, providing cross references to the legislative texts and the analysis in the first part.
The development, manufacture and marketing of pharmaceuticals is a global business - companies in this sector function on a truly international basis and therefore their in-house lawyers and professional advisers must be familiar with the changes and developments that are now taking place in EC law. The pharmaceutical industry is a sector increasingly governed by strict legal restrictions and controls affecting day to day operations. Within Europe, this is taking the form of complex and detailed legislation coming from Brussels as part of the implementation of the Single Market programme. It is at present an area of especially fast moving change in both law and policy. Pharmaceutical companies in Europe are themselves undergoing a major change - in many cases restructuring their production bases, adopting a pan-European approach rather than a purely national one - thus making it all the more important that they understand and have access to the law coming from Brussels. "EC Pharmaceutical Law" is a manual which is designed to provide better use and understanding of this litigation.
It presents the legislation in the first half of the book and then gives detailed commentary in the second half, providing cross references to the legislative texts and the analysis in the first part. "EC Pharmaceutical Law" aims to help the industry protect itself as well as learn about this area of law.

General principles of EC legislation; definition of medical product; authorization and supervision; research and development - manufacturing; intellectual property; pricing; labelling and package leaflets; distribution and supply; marketing; export/import; consumer protection; medical devices; EC legislation - basic legislation, authorization and supervision, research and development: manufacturing, intellectual property, pricing, labelling and package leaflets, distribution and supply, marketing, parallel imports, medical devices.

Erscheint lt. Verlag 16.9.1992
Reihe/Serie European practice library
Zusatzinfo index
Verlagsort Chichester
Sprache englisch
Maße 190 x 250 mm
Gewicht 1240 g
Themenwelt Medizin / Pharmazie Pharmazie
Recht / Steuern EU / Internationales Recht
Technik
Wirtschaft
ISBN-10 0-471-93648-0 / 0471936480
ISBN-13 978-0-471-93648-0 / 9780471936480
Zustand Neuware
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