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Trivalent Seasonal Influenza Vaccine Production (SH 2027)

Open
International

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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This subcontract involves the manufacture and supply of trivalent Seasonal Influenza Virus Vaccines for the Southern Hemisphere 2027 season to support prime contractors fulfilling UNICEF supply contracts. The selected provider is responsible for the entire production cycle, including bulk production, formulation, filling, and labeling. Acceptable manufacturing methods include egg-based, cell culture, recombinant protein, or nucleic acid-based processes, provided the facility possesses the necessary bioreactors or egg-incubation infrastructure and maintains WHO Pre-qualification. The scope of delivery requires the provision of 2,250 10-dose vials and 100 1-dose vials. Performance for this contract will take place across multiple destinations to meet the distribution needs of the agency. The opportunity was posted on November 9, 2026, under NAICS code 325414.

General Info

Manufacture and supply of trivalent influenza vaccines for Southern Hemisphere 2027 UNICEF contracts.

Agency

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of RFP-DAN-2026-503974.

The full solicitation package (4 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

Seasonal Influenza Virus Vaccine, Southern Hemisphere Influenza Season 2027 Luis Roberto Mena - [email hidden]

AI Contract Breakdown

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Timeline

Posted

subcontract

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Organization & Contact Information

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AgencyUNICEF
ContactsNo contacts available
OfficeN/A
Organization / AgencyUNICEF
Office AddressN/A
ContactsNo contact information available

Full Description

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Manufactures and supplies trivalent Seasonal Influenza Virus Vaccines for prime contractors delivering UNICEF supply contracts for the Southern Hemisphere 2027 season. Performs bulk production, formulation, filling, and labeling using egg-based, cell culture, recombinant protein, or nucleic acid-based methods. Requires bioreactors or egg-incubation facilities and WHO Pre-qualification. Delivers 2,250 10-dose vials and 100 1-dose vials.

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