Assistant Professor, Department of Pharmaceutical Sciences, Faculty of Health Sciences, Marwadi University, Rajkot, India.
Professor and Principal, School of Pharmacy, Rai University, Ahmedabad, Gujarat, India.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2024 Jul 18;40:e20240005. doi: 10.62958/j.cjap.2024.005.
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.
制药行业必须保持严格的质量保证标准,以确保产品安全和法规合规。众所周知的六西格玛方法在流程改进和质量控制方面的一个关键组成部分是精确和全面的文件记录。然而,传统文件记录程序存在许多重大问题,包括速度慢、人为错误以及难以符合监管标准。本综述研究探讨了在制药领域采用机器学习 (ML) 和人工智能 (AI) 来增强六西格玛文件记录流程的创新方法。AI 和 ML 提供了先进的技术,有可能通过自动化数据输入、收集和分析来彻底改变文件记录流程。自然语言处理 (NLP) 和计算机视觉技术有可能显著降低人为错误率并提高文件记录流程的效率。通过应用机器学习算法来支持实时数据分析、预测分析和主动质量管理,制药组织可以更早地发现潜在的质量问题,并采取主动措施加以解决。将 AI 和 ML 相结合可以提高文档的准确性和可靠性,同时加强对严格监管标准的遵守。本研究确定了制药行业中当前六西格玛文件记录的主要障碍和限制。它研究了 AI 和 ML 的基础,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好处。报告包括广泛的案例研究,突出了显著的发展,并解释了如何在现实世界中使用 AI/ML 增强文档记录。