Quality Standards for Antiretrovirals in Indian Pharmacopoeia

K. Vivekanandan, H. Sharma, G. Singh
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Abstract

The global antiretroviral market is expanding dramatically with the approval of competent authorities in individual countries. In India, the Central Drugs Standard Control Organization (CDSCO) and Indian Pharmacopoeia Commission (IPC) are making efforts to approve and set the standards for antiretroviral drugs, respectively. The IPC publishes an official book of standards known as Indian Pharmacopoeia ( IP ) in fulfillment of the requirements of the Drugs and Cosmetics Act of 1940. There are 41 antiretroviral active pharmaceutical ingredients (APIs) and combinations approved by the CDSCO; the sixth edition of IP contains 52 monographs of different APIs and formulations. The monographs of antiretrovirals include descriptions, identifications, impurities, assays, and specific tests. IP plays a significant role in improving the quality of antiretroviral drugs, which in turn promote public health.
印度药典中抗逆转录病毒药物的质量标准
在各国主管当局的批准下,全球抗逆转录病毒市场正在急剧扩大。在印度,中央药物标准控制组织(CDSCO)和印度药典委员会(IPC)正在分别努力批准和制定抗逆转录病毒药物的标准。IPC根据1940年《药品和化妆品法》的要求,出版了一本名为《印度药典》的官方标准书。CDSCO批准了41种抗逆转录病毒活性药物成分(api)和组合;IP第六版收录了52篇不同原料药和配方的专著。抗逆转录病毒药物的专著包括描述、鉴定、杂质、测定和特异性试验。知识产权在提高抗逆转录病毒药物的质量方面发挥重要作用,从而促进公共卫生。
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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