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Medicines distribution in Romania in the context of global market

机译:全球市场背景下罗马尼亚的药品分销

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The medicine definitions differ from a country to another; finding a certain definition to be appropriate for the analysis from the perspective of the thematic issue of the present paper has become a necessity. As a first defining characteristic, it has to be pointed out that the medicine is not like the other commodities. It is meant for the most intimate human needs, thus affecting the quality of life, welfare, but also malady, death or human being cure (J.P. Buisson si D. Giorgi, 1997). Consequently, the medicine may be assimilated to a public cvasi-commodity (or under trusteeship), a fact proved by the public authorities attitude which include it into the political or sanitary (D. Richard si J. L. Senon, 1996) and establish organizations to control the supply and demand of medicines. This definition emphasizes the fact that the medicine offer is under trusteeship and regulated throughout the entire chain of value, at least on five levels: 1. Research (research labs must be in accordance with a certain number of international regulations), 2. Manufacturing (production process must respect the 'Good practices of production), 3. Marketing authorization released by the trusteeship authority, 4. Medicine including into its category of accessibility and 5. Medical staff which becomes the real decision maker with regard to medicine administration. All these regulations imposed internationally and supported by OMS influence considerably the medicine production and distribution. That is why the analysis of medicine distribution on a national market cannot be done without taking into account the international market characteristics. In such perspective, the present paper was structured in three sections: (1) Characteristics of medicines global (2) Organizing the system for distribution of medicine in Romania (3) New challenges of distribution of medicinal in Romania
机译:药物定义因国家而异。从本文的主题问题的角度寻找一个合适的定义来进行分析已成为必要。作为第一个定义特征,必须指出该药与其他商品不同。它的目的是满足最紧迫的人类需求,从而影响生活质量,福利,疾病,死亡或人类治愈(J.P. Buisson si D. Giorgi,1997)。因此,该药可能会被同化为一种公共肉类商品(或受托管理),这是由公共当局的态度证明的,并将其纳入政治或卫生领域(D. Richard si JL Senon,1996)并建立了组织来控制药品的供求关系。该定义强调了这样一个事实,即药品的提供受托并在整个价值链中受到监管,至少在五个层面上:1.研究(研究实验室必须符合一定数量的国际法规),2.制造(生产过程中必须遵守“生产的良好实践”。3.托管机构发布的市场营销授权; 4.药品(包括在其可及性类别中); 5.医务人员,这是药品管理的真正决策者。所有这些在国际上强加并由OMS支持的法规都极大地影响了药品的生产和分销。这就是为什么在不考虑国际市场特征的情况下就无法对国内市场上的药品分布进行分析的原因。从这种角度来看,本论文分为三个部分:(1)全球药品的特点(2)在罗马尼亚组织药品分销系统(3)罗马尼亚药品分销的新挑战

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