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水针剂的质量控制:药品生产质量管理规范与外部中药房标准的比较研究

Quality Control of Pharmacopuncture: A Comparative Study of Good Manufacturing Practice and External Herbal Dispensary Standards.

作者信息

Han Ji-Eun, Park Minjung, An Tteul-E-Bom, Park Jong-Hyun, Oh Danny, Kim Kyeong Han, Sung Soo-Hyun

机构信息

Department of Policy Development, National Development Institute of Korean Medicine, Seoul, Republic of Korea.

National Agency for Development of Innovative Technologies in Korean Medicine, Seoul, Republic of Korea.

出版信息

J Pharmacopuncture. 2021 Jun 30;24(2):59-67. doi: 10.3831/KPI.2021.24.2.59.

Abstract

OBJECTIVES

We aimed to compare the external herbal dispensary (EHD) evaluation criteria for pharmacopuncture and the Korea Good Manufacturing Practice (KGMP) sterile medicine standards to contribute to the establishment of quality control criteria for pharmacopuncture.

METHODS

We obtained the KGMP standards from the Ministry of Food and Drug Safety and the pharmacopuncture certification criteria from the Ministry of Health and Welfare of South Korea. The EHD evaluation items were classified into three categories facilities, quality control, and validation. The evaluation items were compared with the KGMP sterile medicine criteria to determine their conformance with each other, followed by a discussion among the committee of six experts and their consensus to suggest the items to complement the EHD evaluation criteria.

RESULTS

Among the KGMP sterile medicine criteria, 44 were related to the management of the facilities, and 32 pharmacopuncture evaluation items corresponded to these KGMP items (66.7%). Fifty-eight KGMP criteria were related to quality management, and 42 pharmacopuncture evaluation items corresponded to these KGMP items (72.4%). Twenty-five KGMP sterile medicine criteria were related to validation, and 11 pharmacopuncture evaluation items corresponded to these KGMP items (44.0%). Sixteen items under the pharmacopuncture EHD criteria corresponded to the KGMP sterile medicine criteria based on the consent of the experts. Among these, 4 were related to facility management, 6 were related to quality control, and 6 were related to validation.

CONCLUSION

For the safety and quality control of pharmacopuncture, there is a need to select the criteria for the mandatory items among the proposed pharmacopuncture-EHD criteria laws and systems to ensure that the pharmacopuncture materials are produced under the pharmacopuncture-EHD in compliance with the relevant requirements. More studies are needed to secure the safety level of pharmacopuncture materials corresponding to that of conventional medicine.

摘要

目的

我们旨在比较药物针灸的外部草药配药室(EHD)评估标准与韩国药品生产质量管理规范(KGMP)无菌药品标准,以促进药物针灸质量控制标准的建立。

方法

我们从韩国食品药品安全部获取了KGMP标准,并从韩国卫生福利部获取了药物针灸认证标准。EHD评估项目分为设施、质量控制和验证三类。将评估项目与KGMP无菌药品标准进行比较,以确定它们之间的一致性,随后由六名专家组成的委员会进行讨论并达成共识,以提出补充EHD评估标准的项目。

结果

在KGMP无菌药品标准中,44项与设施管理相关,32项药物针灸评估项目与这些KGMP项目相对应(66.7%)。58项KGMP标准与质量管理相关,42项药物针灸评估项目与这些KGMP项目相对应(72.4%)。25项KGMP无菌药品标准与验证相关,11项药物针灸评估项目与这些KGMP项目相对应(44.0%)。根据专家的同意,药物针灸EHD标准下的16项与KGMP无菌药品标准相对应。其中,4项与设施管理相关,6项与质量控制相关,6项与验证相关。

结论

为了药物针灸的安全和质量控制,有必要在提议的药物针灸-EHD标准法律和制度中选择强制性项目的标准,以确保药物针灸材料在符合相关要求的药物针灸-EHD下生产。需要更多的研究来确保药物针灸材料的安全水平与传统药物相当。

相似文献

7
History of Research on Pharmacopuncture in Korea.韩国药物针灸研究史。
J Pharmacopuncture. 2016 Jun;19(2):101-8. doi: 10.3831/KPI.2016.19.010.

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