Aurora MMS System, Software and Installation
Closed Pre-Solicitation Posted
- Solicitation number
- NOI-NIAID-24-2228865
- Agency
-
National Institute of Allergy and Infectious Diseases
National Institutes of Health, Department of Health and Human Services
- Responses due
- Set-aside
- No set-aside
Opportunity facts
- NAICS code
- 334516 Analytical Laboratory Instrument Manufacturing
- PSC
- 6640 Laboratory Equipment And Supplies
- Place of performance
- Gaithersburg, Maryland 20878, United States
- Points of contact
Notice details come from SAM.gov. Updated .
About this opportunity
Paragraph 1:
The National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) intends to negotiate on an other than full and open competition basis with Redshift Bio located in Boxborough, MA to procure an Aurora MMS system, software, and installation. The requirements include high-throughput data acquisition of liquid samples, automated sample analysis, advanced data analysis software, and the ability to detect 1% protein secondary structure differences. Interested parties must submit capability statements addressing the specified requirements and catalog numbers by July 1, 2024, 4:00 pm EST.
Paragraph 2:
This procurement is not set aside for any particular program. Redshift Bio is the sole source for the required system as there are no other comparable instruments on the market capable of meeting the specified capabilities. The contract value is not provided, but the solicitation outlines the required quantities, including 1 Aurora MMS system, 1 Aurora upgrade, 3 Aurora-delta software licenses, 1 training session, and 1 installation service, all to be delivered to Gaithersburg, MD.
Notice text
This is a Notice of Intent, not a request for proposal. The National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) intends to negotiate on an other than full and open competition basis with Redshift Bio located in Boxborough, MA to procure an Aurora MMS system, software and installation.
1) Aurora MMS System CATALOG # RSB500-501 QTY: 1
2) Aurora Upgrad e--TX CATALOG # RSB500-528 QTY: 1
3) Aurora-delta (offline) software licenses CAT # RSB500-511 QTY: 3
4) Aurora initial onsite system and applications training CAT # RSB500-522 QTY: 1 A
5) Aurora System installation CAT # RSB500-524 QTY:1
6) Shipping to 9 West Watkins Road, Gaithersburg, MD 20878 FOB DESTINATION
specified requirements.
1. High throughput data acquisition of liquid samples (minimum 30 samples per plate or loading mechanism, plate format preferred)
2. Automated sample analysis (capable of continuous ample analysis without additional user input or monitoring)
3. Software package containing data analysis capabilities including: Second derivative analysis, derivative difference analysis, weighted spectral difference (WSD) analysis, Gaussian spectral deconvolution (required due to variability of vaccines developed at the VPP)*
4. Identification of protein secondary structure differences of (at minimum) 1%*
5. Ability to detect 1% protein secondary structure differences in the presence of common interfering buffer components*
6. Spectral area repeatability ≥ 98%
7. Thermal ramp capabilities between 25/Ambient and 90C
8. Spectral range of (minimum) 1775 to 1580 cm-1
9. Sample volume ≤ 50 uL
10. Sample concentration range of 0.2 to 150 mg/mL (to accommodate all VRC clinical product formats)
11. Footprint < 30” W x 30” D, to fit in current facilities
12. Liquid nitrogen free MCT detector.
Sole Source Justification: There are currently no other comparable instruments on the market by any other vendors that are capable of high-throughput standard and thermal ramp analysis of protein secondary structure in liquid samples aside from the Redshift Bio Aurora MMS-IR. No other manufacturers of Infrared spectrophotometers capable of automated, low-volume, high concentration liquid sample analysis was identified.
Any capability statements submitted MUST address all specified requirements and catalog numbers listed within this posting for consideration.
The statutory authority for this sole source requirement is 41 U.S.C. 1901 (a) (1) as implemented by FAR 13.106-1 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 these kits may submit a capability statement that will be considered by email (subject line to reference NOI-NIAID-24-2228865 to Diana Rohlman at diana.rohlman@nih.gov by July 1, 2024, 4:00 pm eastern standard time.
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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