Vidor Emmanuel, Soubeyrand Benoit
a Medical Affairs , Sanofi Pasteur , Lyon , France.
b Medical Affairs , Sanofi Pasteur MSD , Lyon , France.
Expert Rev Vaccines. 2016 Dec;15(12):1575-1582. doi: 10.1080/14760584.2016.1205492. Epub 2016 Jul 6.
The manufacture of DTP-backboned combination vaccines is complex, and vaccine quality is evaluated by both batch composition and conformance of manufacturing history. Since their first availability, both the manufacturing regulations for DTP combination vaccines and their demand have evolved significantly. This has resulted in a constant need to modify manufacturing and quality control processes. Areas covered: Regulations that govern the manufacture of complex vaccines can be inconsistent between countries and need to be aligned with the regulatory requirements that apply in all countries of distribution. Changes in product mix and quantities can lead to uncertainty in vaccine supply maintenance. These problems are discussed in the context of the importance of these products as essential public health tools. Expert commentary: Increasing demand for complex vaccines globally has led to problems in supply due to intrinsically complex manufacturing and regulatory procedures. Vaccine manufacturers are fully engaged in the resolution of these challenges, but currently changes in demand need ideally to be anticipated approximately 3 years in advance due to long production cycle times.
白喉-破伤风-百日咳(DTP)三联基础组合疫苗的生产复杂,疫苗质量通过批次组成和生产历史的合规性进行评估。自首次上市以来,DTP组合疫苗的生产法规及其需求都发生了显著变化。这导致不断需要修改生产和质量控制流程。涵盖领域:各国管理复杂疫苗生产的法规可能不一致,需要与适用于所有分销国家的监管要求保持一致。产品组合和数量的变化可能导致疫苗供应维持的不确定性。在这些产品作为基本公共卫生工具的重要性背景下讨论了这些问题。专家评论:全球对复杂疫苗的需求增加,由于其内在复杂的生产和监管程序导致了供应问题。疫苗制造商全力应对这些挑战,但由于生产周期长,目前理想情况下需求变化应提前约3年预测。