Intent to Sole Source - Endotoxin Detection System Cartridges
| Agency: | HEALTH AND HUMAN SERVICES, DEPARTMENT OF |
|---|---|
| State: | Maryland |
| Type of Government: | Federal |
| FSC Category: |
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| NAICS Category: |
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| Set Aside: | No Set aside used |
| Posted Date: | Aug 4, 2026 |
| Due Date: | Aug 7, 2026 |
| Solicitation No: | NOI-CC-OLAO-26-007979 |
| Original Source: | Please Login to View Page |
| Contact information: | Please Login to View Page |
| Bid Documents: | Please Login to View Page |
Description
- Contract Opportunity Type: Special Notice (Original)
- Original Published Date: Aug 04, 2026 10:18 am EDT
- Original Response Date: Aug 07, 2026 12:00 pm EDT
- Inactive Policy: 15 days after response date
- Original Inactive Date: Aug 22, 2026
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Initiative:
- None
- Original Set Aside: No Set aside used
- Product Service Code: 6640 - LABORATORY EQUIPMENT AND SUPPLIES
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NAICS Code:
- 325414 - Biological Product (except Diagnostic) Manufacturing
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Place of Performance:
Bethesda , MD 20892USA
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: Charles River Laboratories.
Acquisition Description:
The PET Radiopharmacy uses Charles River Laboratories’ FDA licensed endotoxin detection system, a portable testing system (PTS) to ensure all manufactured PET IND products are pyrogen-free prior to release. The PTS utilizes disposable cartridges unique to the system. At least one cartridge is needed for every PET IND produced.
The endotoxin detection system cartridges are estimated to cost $22,200 and is required to be delivered by 08/24/2026.
The PTS and cartridges are used for bacterial endotoxin testing required for each PET IND produced.
Because of the proprietary of these cartridges to our PTS units, only one source is solicited. The cartridges must be delivered by 02/01/2025. If the required delivery date is not met, there will not be enough cartridges available to perform testing required to release of PET IND products for patient 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-CC-OLAO-26-007979) by 12:00 PM eastern standard time on 08/07/2026 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.
- 3100 Center Drive Room 1B59
- Bethesda , MD 20892
- US
- Aug 04, 2026 10:18 am EDTSpecial Notice (Original)
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