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当某些国家的市场受到违法及不合格药品的不良影响时,有关责任者有义务积极宣传并履行世界卫生组织针对国际贸易制订的药品质量证书规范,从而保障经销药品在国际贸易中的信誉。为了切实地实施这个规范,必须对它准确而清晰地加以说明,以使有关人员对该规范的目的与要求有一个全面了解。在前几期世界卫生组织药品报道资料中,对其执行情况和作用曾作过详细的叙述,下面再次强调说明其基本原则,以进一步消除可能的误解。无论来自政府方面,还是制药工业方面,涉及本规范的任何人员对改进该规
When the market in some countries is adversely affected by unlawful and unqualified drugs, the relevant responsible persons are obliged to actively promote and fulfill the norms of quality certificates issued by the World Health Organization for international trade so as to ensure the credibility of the pharmaceutical products in international trade. In order to implement this code effectively, it must be accurately and clearly described so that the relevant personnel have a comprehensive understanding of the purpose and requirements of the code. In the previous WHO drug reports, detailed descriptions of its implementation and its role have been made, and the following re-emphasizes its basic principles in order to further eliminate possible misunderstandings. Whether it comes from the government, or the pharmaceutical industry, any person involved in this code to improve the regulation