Quality Culture and Knowledge Management in the Japanese Pharmaceutical Industry-A Cross-Sectional Study and Case Report.

Q3 Medicine PDA Journal of Pharmaceutical Science and Technology Pub Date : 2023-09-01 Epub Date: 2023-06-15 DOI:10.5731/pdajpst.2022.012797
Shiho Takahashi, Tetsuhito Takarada, Kanako Ito, Mayumi Shikano, Shingou Sakurai
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Abstract

In the past few years, there have been several instances of illicit pharmaceutical manufacturing in Japan. Insufficient good manufacturing practice compliance and lack of quality culture in some pharmaceutical companies have been suggested as the underlying reasons for such cases. We aimed to focus on knowledge management and fostering of quality culture in pharmaceutical companies in Japan to understand their current situation and find a strategy for the availability of high-quality reliable pharmaceutical products. A wide-ranging questionnaire survey was conducted to understand the issues related to knowledge management and fostering of quality culture across pharmaceutical companies in Japan. A published investigation report on an illicit manufacturing case was closely examined by organizing the available facts using the diagram. Based on 395 responses to the questionnaire survey, we found that although pharmaceutical companies understand the importance of knowledge management and quality culture, issues exist in their operational methods. A total of 94% of the respondents agreed that they mentioned "knowledge management" as an enabler of the Pharmaceutical Quality System of ICH Q10, and 98% of the respondents accepted that insufficient fostering of quality culture leads to corporate risk. However, the survey revealed that many companies are struggling with this approach. Based on a report on an illicit manufacturing case, we analyzed the direct causes of misconduct and prepared a systematic summary that can be easily comprehended. Comparison of the illicit manufacturing case report with our questionnaire results suggests that many pharmaceutical companies do not regard the misconduct case as a situation that could occur in their company. With the revision of the Pharmaceuticals and Medical Devices Act and good manufacturing practice Ministerial Ordinance, we advocate the need for all employees of pharmaceutical companies to reconsider the priorities of their companies from the patient perspective.

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日本制药行业的质量文化和知识管理——一个横断面研究和案例报告。
在过去几年中,日本发生了几起非法制药事件。一些制药公司的良好生产规范合规性不足和缺乏质量文化被认为是此类案件的根本原因。我们的目标是专注于知识管理和培养日本制药公司的质量文化,以了解他们的现状,并找到提供高质量可靠药品的战略。进行了一项广泛的问卷调查,以了解日本制药公司在知识管理和培养质量文化方面的问题。通过使用图表整理现有事实,对一份已公布的关于非法制造案件的调查报告进行了仔细审查。基于395份问卷调查,我们发现,尽管制药公司了解知识管理和质量文化的重要性,但其运营方法存在问题。共有94%的受访者同意他们提到“知识管理”是ICH Q10药品质量体系的推动者,98%的受访者认为质量文化培养不足会导致企业风险。然而,调查显示,许多公司都在努力采用这种方法。根据一份关于非法制造案件的报告,我们分析了不当行为的直接原因,并编写了一份易于理解的系统总结。将非法制造案件报告与我们的问卷调查结果进行比较表明,许多制药公司并不认为不当行为案件是其公司可能发生的情况。随着《药品和医疗器械法》和《良好生产规范部长条例》的修订,我们主张制药公司的所有员工都需要从患者的角度重新考虑公司的优先事项。
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CiteScore
1.90
自引率
0.00%
发文量
34
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