简化监管事务中的变更控制流程:最佳实践与案例研究

Sri Sai Subramanyam Challa, Abhip Dilip Chawda, Abhishek Pandurang Benke, Mitul Tilala
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引用次数: 0

摘要

变更控制是各行各业监管事务的重要组成部分,尤其是在制药、医疗器械和生物技术领域。本研究论文探讨了与传统变更控制流程相关的挑战,并介绍了简化这些流程以提高效率、合规性和整体产品质量的最佳实践。通过全面的文献综述和对领先企业案例的分析,我们确定了优化变更控制工作流程、利用技术和培养持续改进文化的关键策略。本文还探讨了简化变更控制流程对合规性、产品生命周期管理和组织绩效的影响。我们的研究结果表明,实施这些最佳实践可以大大缩短变更实施时间,改善监管合规性,提高产品质量和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Streamlining Change Control Processes in Regulatory Affairs: Best Practices and Case Studies
Change control is a critical component of regulatory affairs in various industries, particularly in pharmaceuticals, medical devices, and biotechnology. This research paper explores the challenges associated with traditional change control processes and presents best practices for streamlining these processes to improve efficiency, compliance, and overall product quality. Through a comprehensive literature review and analysis of case studies from leading organizations, we identify key strategies for optimizing change control workflows, leveraging technology, and fostering a culture of continuous improvement. The paper also examines the impact of streamlined change control processes on regulatory compliance, product lifecycle management, and organizational performance. Our findings suggest that implementing these best practices can lead to significant reductions in change implementation time, improved regulatory compliance, and enhanced product quality and safety.
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