Task V09: Development and Manufacture of Toxoid Fusion Master Banks

传染病疫苗和其他生物制品的制造和表征服务(MCS)合同提供各种服务，包括产品开发规划和可行性评估；产品优化；I/II期临床研究的产品开发和符合cGMP的生产；技术和设施审计；以及适用于提交给美国食品和药物管理局(FDA)的监管支持。这些服务将促进开发和引入新的疫苗和生物制品，以应对生物恐怖主义和新出现和重新出现的传染病的潜在病原体。该合同还规定了疫苗、包括佐剂在内的疫苗组件、疫苗输送系统、其他生物制品和挑战材料的制造。

The Manufacture and Characterization Services (MCS) for Vaccines and Other Biologics for Infectious Diseases contract provides a variety of services spanning product development planning and feasibility assessments; product optimization; product development and cGMP compliant manufacture for Phase I/II clinical studies; technical and facility audits; and regulatory support appropriate for submission to the U.S. Food and Drug Administration (FDA). These services will facilitate the development and introduction of new vaccines and biologics against potential agents of bioterrorism and emerging and re-emerging infectious diseases. This contract also provides for manufacture of vaccines, vaccine components including adjuvants, vaccine delivery systems, other biologics, and challenge material.