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Quadrivalent Influenza Vaccine Supply (Contingency Option)

Active

Federal

Response Deadline09/08/2026, 07:30:00 PM UTC

Contract Overview

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

AI Contract Overview

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Nac Pharmaceuticals, under the Department of Veterans Affairs, is seeking a subcontract for the contingency supply of quadrivalent influenza vaccines suitable for all age groups. This procurement is triggered specifically if the World Health Organization recommends the quadrivalent version and trivalent vaccines are unavailable. All supplied vaccines must maintain full FDA labeling and adhere to current Good Manufacturing Practice compliance. The solicitation was posted on August 25, 2026, with a response deadline of September 8, 2026. This requirement falls under NAICS code 325413 for pharmaceutical preparation.

General Info

Nac Pharmaceuticals seeks subcontracts for contingency quadrivalent influenza vaccines for Veterans Affairs.

Agency

Department Of Veterans Affairs → Nac Pharmaceuticals (36E797)View Agency

NAICS

325413 - In-Vitro Diagnostic Substance ManufacturingView NAICS

Place of Performance

IL

Set-Aside

NONE

Documents

This scope was carved out of 36E79726R0035.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

6505--2027-2028 Influenza Virus Vaccine

AI Contract Breakdown

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Timeline

PostedAug 25

subcontract

Response DeadlineSep 8

Submission deadline

Response Deadline

09/08/2026, 07:30:00 PM UTCin 10 days

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → Nac Pharmaceuticals (36E797)

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Veterans Affairs → Nac Pharmaceuticals (36E797)

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Office AddressN/A

ContactsNo contact information available

Full Description

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Contingency supply of quadrivalent influenza vaccine for all age groups if WHO recommends it and trivalent is unavailable, with full FDA labeling and cGMP compliance.

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