Vaccine Antigen and Adjuvant Manufacturing
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The contract pertains to the manufacture of bulk influenza vaccine antigens and adjuvanted formulations in compliance with current good manufacturing practices for use in clinical trials and emergency response scenarios. The work must adhere to stringent quality and regulatory standards to ensure safety and efficacy, with production intended to support public health preparedness and rapid deployment during outbreaks. The place of performance is designated as Washington, DC, with a delivery deadline for responses set for August 15, 2026. This subcontract falls under the NAICS code 325412, indicating classification within pharmaceutical and medicine manufacturing, and is issued by the Biomedical Advanced Research and Development Authority under the Department of Health and Human Services. Participation requires capability to scale production while maintaining cGMP compliance across all stages of antigen and adjuvant formulation, with no set-aside provisions specified for small or disadvantaged businesses.
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Washington, DC, 20024, USASet-Aside
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