药物警戒是药物监管系统的关键组成部分

Farmacevticheskoe delo i tehnologija lekarstv (Pharmacy and Pharmaceutical Technology) Pub Date : 2022-06-15 DOI:10.33920/med-13-2206-02

Igor Valerievich Korobkin

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引用次数: 0

摘要

对分配风险类别的控制对象的信息进行收集、处理、分析和记录。药品生产企业与产品接收方签订交换产品安全数据的协议，以识别和研究可能存在的使用安全问题，并确认对投入流通的药品安全的社会责任。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Pharmacovigilance as a key component of drug regulatory systems

Information for control objects that are assigned risk categories is collected, processed, analyzed and recorded. The pharmaceutical manufacturer enters into an agreement with the recipient of the products on the exchange of data on the safety of such products in order to identify and study possible problems related to the safety of use, as well as to confirm social responsibility for the safety of drugs put into circulation.

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Farmacevticheskoe delo i tehnologija lekarstv (Pharmacy and Pharmaceutical Technology)

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