仿制药杂志-社论2021年12月

B. Tempest
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引用次数: 0

摘要

在疫情关闭后,FDA于2021年9月左右重新开始对印度工厂进行检查,印度和美国FDA办公室的代表都出席了检查。对于2021年底在美国FDA注册的仿制药设施,印度仍然拥有最多的活性药物成分(API)生产设施(183个)。继2021年上半年仿制药价格下调后,美国药品价格似乎在上一季度企稳。[摘自文章]《Journal of Generic Medicines》的版权是Sage Publications Inc.的财产,未经版权所有者的明确书面许可,其内容不得复制或通过电子邮件发送到多个网站或发布到listserv。但是,用户可以打印、下载或通过电子邮件发送文章供个人使用。这可以删节。对副本的准确性不作任何保证。用户应参阅原始出版版本的材料的完整。(版权适用于所有人。)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Journal of Generic Medicine – Editorial December 2021
Inspections by the FDA of Indian plants restarted around September 2021 after the pandemic shutdown with representatives from both the Indian and USA FDA offices in attendance. For generic drug facilities registered with the USA FDA at the end of 2021, India continues to have the largest number of Active Pharmaceutical Ingredient (API) manufacturing facilities (183). After the lowering of generic medicine prices in the first half of 2021, USA medicines prices seem to have stabilised in the last quarter. [Extracted from the article] Copyright of Journal of Generic Medicines is the property of Sage Publications Inc. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)
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