Specific Anti-Alpha-Gal ImmunoCAPTM Phadia Core Laboratory Testing (ThermoFisher Scientific) for Research Blood Donors

Closed Special Notice Posted

Solicitation number
NOI-CC-OLAO-26-008249
Agency
Responses due
Set-aside
No set-aside

Opportunity facts

Place of performance
Bethesda, Maryland 20892, United States

Notice details come from SAM.gov. Updated .

About this opportunity

The National Institute of Health, Clinical Center issued a notice of intent on July 23, 2026 to negotiate on a sole-source basis with ThermoFisher Scientific for Phadia Immunology Reference Laboratory testing services; the Government reserves discretion to compete the requirement based on capability statements received by August 2, 2026 at 12:00 PM Eastern time.

The requirement covers anti-alpha-gal and total immunoglobulin E (IgE) testing for research blood donors through ThermoFisher Scientific's Phadia Core Laboratory, which optimizes workflows for allergy and autoimmune diagnostics with calibrated, reliable testing data and improved turnaround time for clinical and research use. The sole-source determination rests on statutory authority under 41 U.S.C. 253(c)(1) as implemented by FAR 6.302-1, citing one responsible source and no other adequate supply or service.

Responsible sources may submit a capability statement by email to valerie.gregorio@nih.gov with subject line NOI-OLAO-CC-26-008249 by the August 2 deadline. All responses received by the closing date will be considered; the Government retains sole discretion to determine whether to compete the requirement.

Notice text

This is a Notice of Intent, not a request for proposal.  The National Institute of Health, Clinical Center (NIH-CC) intends to negotiate on an other than full and open competition basis with the following vendor: Phadia

Acquisition Description:

ThermoFisher Scientific Phadia Immunology Reference Laboratory (PiRL), optimizes laboratory workflows for allergy and autoimmune diagnostics including alpha-gal and total immunoglobulin E (IgE), providing calibrated, reliable testing data with efficiency and improved turnaround time for clinical and research use.

The statutory authority for this sole source requirement is 41 U.S.C. 253(c) (1) as implemented by FAR 6.302-1 only one responsible source and no other supply of service will satisfy agency requirements. THIS IS NOT A REQUEST FOR PROPOSAL.  All responsible sources that could provide the required may submit a capability statement that will be considered by email (subject line to reference NOI-OLAO-CC-26-008249) by 12:00 PM eastern standard time on 08/2/2026 to: valerie.gregorio@nih.gov.

All responses received by the closing date of this synopsis will be considered by the Government.  A determination not to compete this requirement, based upon responses to this notice, is solely within the discretion of the Government.

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