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Notice to applicants for marketing authorizations for proprietary medicinal products in the Member States of the European Community on the use of the new multi-state procedure created by Council Directive 83/570/EEC

机译：关于使用由理事会指令83/570 / EEC创建的新的多州程序的欧洲共同体成员国的专利医药产品营销许可申请人的通知

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1. Marketing of medicinal products in the European Community. The Mutual Recognition and Decentralised Procedures. [J] . Bachmann P Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz . 2008,第7期

机译：在欧洲共同体的药品销售。相互承认和分散程序。
2. The availability of veterinary pharmaceutical products: proposal for a Regulation of the European Parliament and of the Council laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, and repealing Regulation (EEC) No. 2377/90 [J] . Buettner-Peter U. Fleischwirtschaft . 2008,第1期

机译：兽药产品的可用性：欧洲议会和理事会条例的提案，其中规定了建立动物源性食品中药理活性物质残留限量的共同体程序，并废除了第2377/90号法规（EEC）
3. Council Directive 89/105/EEC of 21 December 1988 relating to the transparency of measures regelating the prices of medicinal products for human use and their inclusion in the scope of national health insurance systems [J] . THE COUNCIL OF THE EUROPEAN COMMUNITIES Pharmaceuticals policy and law. . 2011,第3a4期

机译：1988年12月21日理事会指令89/105 / EEC，该指令涉及重新定价用于人类使用的药品价格并将其纳入国家健康保险体系范围的措施的透明度
4. Future System for the Free Movement of Medicial Products in the European Community. Proposal for a Council Regulation (EEC) laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products. Proposal for a Council Directive amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC in respect of medicinal products. Proposal for a Council Directive amending Directives 81/851/EEC and 81/852/EEC in respect of veterinary medicinal products. Proposal for a Council Directive repealing Directive 87/22/EEC on the approximation of national measures relating to the placing on the market of high technology medicinal products particularly those derived from biotechnology. COM (90) 283 final, 14 November 1990 [O] . 1990

机译：欧洲共同体医疗产品自由流动的未来体系。建议理事会条例（EEC）制定共同体授权和监督人类和兽医用药品的程序，并建立欧洲药品评价机构。关于修订关于药品的指令65/65 / EEC，75/318 / EEC和75/319 / EEC的理事会指令的提案。关于修订关于兽药产品的指令81/851 / EEC和81/852 / EEC的理事会指令的提案。关于理事会指令的提案，废除了关于高科技医药产品投放市场的国家措施的近似指令87/22 / EEC，特别是那些来自生物技术的产品。 COm（90）283决赛，1990年11月14日

Notice to applicants for marketing authorizations for proprietary medicinal products in the Member States of the European Community on the use of the new multi-state procedure created by Council Directive 83/570/EEC

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