1992 Planning for the Chemicals, Pharmaceuticals, and Biotechnology

Another in the series of industry-by-industry guides to help companies take full advantage of the economic integration of the European Common Market, now scheduled for 1992. Summarizes the legislation proposed and adopted for the elimination of technical, physical, and fiscal barriers, and the timetable for their implementation. Topics include standards, testing, and certification procedures; research and development; licensing, pricing, and marketing of pharmaceuticals; biotechnology based products; intellectual property, patents, and trademarks; standards of good practice legally required; environmental policy; consumer protection constraints; freedom of establishment for the professions; customs; and corporate issues. No bibliography. No index. Annotation copyright Book News, Inc. Portland, Or.