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Justification 1 notice

Vaccines for Children 75D30125D00195

Solicitation 75D30125D00195 Copied Notice ID f2d9e485bef946efb0c581678f9998f0 Copied HEALTH AND HUMAN SERVICES, DEPARTMENT OF — CDC OFFICE OF ACQUISITION SERVICES
SAM.gov
Posted
Aug 21, 2025
Deadline
No deadline
Set-aside
None
NAICS
325412
PSC
6505

Summary

AI-generated · Aug 24, 2025

Modify the existing pediatric vaccine IDIQ contracts to add Clesrovimab (Enflonsia), a product indicated for prevention of RSV lower respiratory tract disease, hospitalization, and death in neonates and infants entering their first RSV season. The effort will provide about 750,000 doses to supply VFC-eligible neonates and newborns and is planned as a sole-source follow-on to Merck to add Clesrovimab to the contract.

All responsible sources may submit capability statements, proposals, or quotations for consideration.

CDC Office of Acquisition Services awarded multiple indefinite delivery, indefinite quantity (IDIQ) contracts for the National Center for Immunization and Respiratory Diseases (NCIRD) for the purchase of standard commercial pediatric & adult vaccines, manufactured under a current establishment and product license issued by the U.S. Food and Drug Administration (FDA). The vaccines awarded under these contracts will be purchased for NCIRD s immunization awardees (the fifty state health departments, several large city program and current and former U.S. Territories) to support immunization programs as provided under Section 317(j) of the Public Health Service Act and VFC, as established pursuant to Section 13631 of the Omnibus Budget Reconciliation Act of 1993. The initial pediatric contracts, awarded in April 2025 were established to support public sector ACIP recommended routine vaccinations for children. Merck s pediatric contract will be modified to support purchase of Clesrovimab (Enflonsia), which is indicated for the prevention of RSV lower respiratory tract disease, hospitalization, and death in neonates and infants who are born during or entering their first RSV season, in light of the ACIP approval and accompanying VFC resolution on June 25, 2025. Clesrovimab from Merck is the second product currently licensed for the prevention of RSV in neonates and infants to prevent severe RSV disease. CDC s current pediatric contract with Merck will be modified to include ~750,000 doses required to support purchase of Clesrovimab to administer to VFC eligible neonates and newborns. CDC intends on awarding a sole source follow on action to Merck to allow for the addition of Clesrovimab. All responsible sources may submit a capability statement, proposal, or quotation, which shall be considered by the agency.

From Justification posted on Aug 21, 2025

Notice history

1
  1. Justification LATEST Posted Aug 21, 2025 View

Details

Solicitation number 75D30125D00195
Notice ID f2d9e485bef946efb0c581678f9998f0
Award number 75D30125D00195
Notice type Justification
Product / Service (PSC) 6505
NAICS 325412
Place of performance Atlanta, Georgia
Archive date Aug 29, 2025

Award Information

Awardees
0
Award Date
Apr 01, 2025

Documents

No files available

View on SAM.gov

Contacts

primary
James Sprigler

Email

secondary
Chad Turner

Email

Agency

HEALTH AND HUMAN SERVICES, DEPARTMENT OF
CENTERS FOR DISEASE CONTROL AND PREVENTION
CDC OFFICE OF ACQUISITION SERVICES

Place of Performance

Atlanta, Georgia
USA

Dates

Posted Aug 21, 2025 11 months ago
Last Updated Aug 06, 2026 1 day ago
Awarded Apr 01, 2025 1 year ago