文章摘要
李旻,王勇,赵宏哲,周婕,刘雨乐,张呈菊,汤纳平,李华,常艳.新冠疫情对药物非临床研究试验机构的合规性影响及应对策略[J].中国药事,2023,(2):157-162
新冠疫情对药物非临床研究试验机构的合规性影响及应对策略
The Impact of the COVID-19 Epidemic on the Compliance of GLP Test Facilities and the Corresponding Strategies
  
DOI:10.16153/j.1002-7777.2023.02.005
中文关键词: 新冠疫情  GLP遵从性  业务可持续性计划  灾难恢复计划
英文关键词: COVID-19  GLP compliance  BCP  DRP
基金项目:上海市科委研发平台项目(编号 21DZ2291000)
作者单位
李旻 上海益诺思生物技术股份有限公司,上海 201203 
王勇 益诺思生物技术南通有限公司,南通 226133 
赵宏哲 上海益诺思生物技术股份有限公司,上海 201203 
周婕 上海益诺思生物技术股份有限公司,上海 201203 
刘雨乐 大连海事大学,大连 116026 
张呈菊 上海益诺思生物技术股份有限公司,上海 201203 
汤纳平 上海益诺思生物技术股份有限公司,上海 201203 
李华 益诺思生物技术南通有限公司,南通 226133 
常艳 上海益诺思生物技术股份有限公司,上海 201203 
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中文摘要:
      目的:探讨如何提升GLP试验机构应对新冠疫情所带来挑战的管理能力。方法:梳理中国、美国、OECD、英国的GLP监管政策,结合本机构2022年上海疫情实际经历,归纳GLP试验机构降低GLP遵从性的风险管控方法。结果结论:GLP试验机构应着重预案能力的建设(如业务可持续性计划、灾难恢复计划),并从加强自身质量体系建设(如及时优化或新增标准操作规范)、强化技术人员培训等方面提升GLP试验机构管理水平,才能应对各类社会重大突发事件(如新冠疫情)和满足国内外监管机构的要求。
英文摘要:
      Objective: To discuss how to improve the management capacity of GLP test facilities to cope with the challenges posed by the COVID-19 epidemic. Methods: The GLP regulatory policies of China, the United States, OECD and the United Kingdom were sorted out, and the risk management and control methods for GLP test facilities to reduce GLP compliance were summarized in combination with our actual experience of Shanghai COVID-19 epidemic in 2022. Results and Conclusion: GLP test facilities should focus on the construction of emergency response capacity (such as business continuity plan and disaster recovery plan), and improve their management level from aspects such as strengthening their own quality system construction (such as timely optimization or addition of standard operating procedures), strengthening the training of technical personnel, so as to deal with various major social emergencies (such as the new coronal epidemic) and meet the requirements of domestic and foreign regulatory agencies.
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