首页> 中文期刊> 《食品与药品》 >我国血液制品生产监管法律法规历史沿革及发展建议

我国血液制品生产监管法律法规历史沿革及发展建议

         

摘要

血液制品全过程监管是政府监管血液制品安全有效的重要措施.在我国,监管的整体框架已基本建立且日趋合理,但法律法规在科学管理和技术指导等方面仍需进一步完善.本文通过文献研究和专业人士访谈,梳理了血液制品全过程监管的法律法规,概括行业现状,对现阶段政府全过程监管血液制品进行积极有益的探究,并对完善我国血液制品监督管理提出改进建议.%Whole process supervision is the important effective measure to ensure the safety of blood products. In our country, the overall framework of the supervision and administration of blood products has been basically established, and is becoming more and more scientific and reasonable. But the laws and regulations are still not complete in scientific administration and technical guidance. In this paper, the important laws and regulations in whole process supervision of blood products are analyzed through the literature research and interview with professionals. The current status of this industry are also summarized, and the current problems in whole process supervision are explored, thus putting forward proposals for improving the blood products production management in China.

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