Leveraging AI and Machine Learning in Six-Sigma Documentation for Pharmaceutical Quality Assurance.

Mausami Chandrakantbhai Vaghela, Sanjesh Rathi, Rahul L Shirole, Jyoti Verma, Shaheen, Saswati Panigrahi, Shubham Singh
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Abstract

The pharmaceutical industry must maintain stringent quality assurance standards to ensure product safety and regulatory compliance. A key component of the well-known Six Sigma methodology for process improvement and quality control is precise and comprehensive documentation. However, there are a number of significant issues with traditional documentation procedures, including as slowness, human error, and difficulties with regulatory standards. This review research looks at innovative ways to employ machine learning (ML) and artificial intelligence (AI) to enhance Six Sigma documentation processes in the pharmaceutical sector. AI and ML provide cutting-edge technologies that have the potential to drastically alter documentation processes by automating data entry, collection, and analysis. Natural language processing (NLP) and computer vision technologies have the potential to significantly reduce human error rates and increase the efficacy of documentation processes. By applying machine learning algorithms to support real-time data analysis, predictive analytics, and proactive quality management, pharmaceutical organizations may be able to identify potential quality issues early on and take proactive efforts to address them. Combining AI and ML improves documentation accuracy and reliability while also strengthening compliance with stringent regulatory criteria. The primary barriers and limitations to the current state of Six Sigma documentation in the pharmaceutical industry are identified in this study. It examines the fundamentals of AI and ML with an emphasis on their specific applications in quality assurance and potential benefits for Six Sigma processes. The report includes extensive case studies that highlight notable developments and explain how AI/ML enhanced documentation is used in the real world.

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在六西格玛文件中利用人工智能和机器学习,实现药品质量保证。
制药业必须保持严格的质量保证标准,以确保产品安全和符合法规要求。众所周知的六西格玛流程改进和质量控制方法的一个关键组成部分就是精确而全面的文档记录。然而,传统的文档记录程序存在许多重大问题,包括速度缓慢、人为错误以及难以符合监管标准。本综述研究探讨了采用机器学习(ML)和人工智能(AI)加强制药行业六西格玛文档编制流程的创新方法。人工智能和 ML 提供了前沿技术,有可能通过自动化数据录入、收集和分析,极大地改变文档编制流程。自然语言处理(NLP)和计算机视觉技术有可能大大降低人为错误率,提高文档流程的效率。通过应用机器学习算法来支持实时数据分析、预测分析和前瞻性质量管理,制药企业可以及早发现潜在的质量问题,并采取积极措施加以解决。人工智能与 ML 的结合提高了文档的准确性和可靠性,同时也加强了对严格监管标准的合规性。本研究确定了制药行业六西格玛文件编制现状的主要障碍和限制。报告探讨了人工智能和智能语言的基本原理,重点介绍了它们在质量保证方面的具体应用以及对六西格玛流程的潜在益处。报告包括大量案例研究,重点介绍了显著的发展,并解释了在现实世界中如何使用人工智能/ML 增强文档。
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CiteScore
0.70
自引率
0.00%
发文量
53
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