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从不同视角看土耳其制药行业政策的伦理概述

Ethical Overview of Pharmaceutical Industry Policies in Turkey from Various Perspectives.

作者信息

Oral Murat, Özçelikay Gülbin

机构信息

Ankara University, Faculty of Pharmacy, Department of Pharmacy Management, Ankara, Turkey.

出版信息

Turk J Pharm Sci. 2017 Dec;14(3):264-273. doi: 10.4274/tjps.88598. Epub 2017 Nov 20.

Abstract

OBJECTIVES

Countries' national drug policies include all key stakeholders (pharmacists, physicians, pharmaceutical firms, and patients) in the public, the private sector, and the field of pharmacy. The aim of this study was to outline pharmaceutical patents and data protection, orphan drugs, drug pricing, and surplus goods regarding pharmacoeconomics, promotions, inspections in the pharmaceutical industry, and policies in pharmacies with respect to buying and selling drugs, and to discuss ethics in particular.

MATERIALS AND METHODS

Written laws in force relating to drugs in Turkey constitute the materials of this study.

RESULTS

Essential medicines must always be accessible. Both governments and pharmaceutical companies must fulfill the obligations imposed on them in an ethical way. Research and development activities must also be carried out for orphan drugs. While pricing drugs, authorities must take pharmacoeconomic evaluations into account.

CONCLUSION

Drugs must be accessible and in the first grade at all times under all circumstances because a product cannot replace it. The concept of surplus goods should be revised to ensure the common needs of the pharmaceutical industry, warehouses, and pharmacies. Promotions in the field by the pharmaceutical industry should be made based on scientific evidence in an ethical way. Inspectors should perform meticulous pharmaceutical industry inspections.

摘要

目标

各国的国家药品政策涵盖了公共部门、私营部门和药学领域的所有关键利益相关者(药剂师、医生、制药公司和患者)。本研究的目的是概述药物经济学、促销、制药行业检查以及药店药品买卖政策方面的药品专利与数据保护、孤儿药、药品定价和剩余药品,并特别讨论伦理问题。

材料与方法

土耳其现行的与药品相关的成文法构成本研究的材料。

结果

基本药物必须始终可及。政府和制药公司都必须以符合伦理的方式履行各自承担的义务。还必须针对孤儿药开展研发活动。在定价药品时,当局必须考虑药物经济学评估。

结论

在任何情况下,药品必须始终可及且处于一流水平,因为没有其他产品能够替代它。应修订剩余药品的概念,以确保制药行业、仓库和药店的共同需求。制药行业在该领域的促销活动应以科学证据为基础,以符合伦理的方式进行。检查人员应认真开展制药行业检查。

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本文引用的文献

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