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Supply of ELISpot Reader (CTL S6 Entry Analyzer or Equivalent)

Active

Federal

Response Deadline09/03/2026, 07:00:00 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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The Department of Health and Human Services, through the FDA Office of Acquisition and Grant Services, is seeking a subcontract for the procurement and delivery of one Enzyme-linked ImmunoSpot reader. The required equipment must be a CTL S6 Entry Analyzer or a functional equivalent that meets all performance specifications necessary for regulatory research focused on immunogenicity assessment. This opportunity is categorized under NAICS code 334516. Interested parties must submit their responses by the deadline of September 3, 2026, following the posting date of August 25, 2026.

General Info

FDA seeks subcontract for one Enzyme-linked ImmunoSpot reader by September 3, 2026.

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant SvcsView Agency

NAICS

334516 - Analytical Laboratory Instrument ManufacturingView NAICS

Place of Performance

MD, USA

Set-Aside

NONE

Documents

This scope was carved out of 75F40126Q135613.

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

View the prime solicitation

FDA ELISpot Reader

AI Contract Breakdown

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Timeline

PostedAug 25

subcontract

Response DeadlineSep 3

Submission deadline

Response Deadline

09/03/2026, 07:00:00 PM UTCin 8 days

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

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Office AddressN/A

ContactsNo contact information available

Full Description

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Procurement and delivery of one Enzyme-linked ImmunoSpot (ELISpot) reader, specifically a CTL S6 Entry Analyzer or equivalent, meeting all functional and performance requirements for use in regulatory research on immunogenicity assessment.

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