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This Government Contract opportunity from Department Of Health And Human Services was posted on August 27, 2020. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Spex Geno Grinder

Awarded
FDA-20-RFQ-1231748Federal

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The FDA Kansas City Laboratory is seeking to acquire a Spex Geno Grinder to support Multi-Mycotoxin analyses conducted via LC-MS/MS Triple Quadrupole Mass Spectrometry. This equipment is essential for the shaking and homogenization of food products within the agency's Total Diet Study and regulatory programs for domestic and imported human and animal feed. As the laboratory transitions to a single, multi-mycotoxin analysis method, a second unit is required to provide necessary backup and redundancy for their existing seven-year-old equipment. This procurement, identified by solicitation number FDA-20-RFQ-1231748, will be awarded as a firm-fixed price purchase order. The contract will be granted to the responsible offeror providing the most advantageous proposal based on price and other specified factors. The work will be performed in Overland Park, Kansas, under the oversight of the Department of Health and Human Services.

General Info

Contract Value

$15,877.69

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

Overland Park, KS, 66214, USA

Set-Aside

NONE

Award Issued Date

Documents

1

RFQ1231748+Spex+Geno+Grinder.docx

DOCX

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Timeline

PhaseAwarded
Posted

Combined Synopsis

Awarded

Contract was awarded

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Contacts1 person available
OfficeBeltsville, MD, 20705, USA
Office AddressBeltsville, MD, 20705, USA
Contacts
Todd Johnston

Full Description

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The Food and Drug Administration, Kansas City Laboratory (11510 W 80th St, Lenexa, KS 66214) performs Multi-Mycotoxin analyses using LC-MS/MS Triple Quadrupole Mass Spectrometry as part of the agency's Total Diet Study and mycotoxin regulatory programs in both domestic and import human and animal feed. The procedure used for this analysis requires a Geno/Grinder for adequate sample extraction (ie., shaking and homogenization of food products). The laboratory is transitioning from the use of individual analyte methods for all samples to the use of the single, multi-mycotoxin analysis. The lab currently has one seven year old Geno/Grinder which is used for the procedures. A second unit is needed to provide equipment backup and redundancy in this critical work area. The Government intends to award a firm-fixed price purchase order resulting from this solicitation to the responsible offeror whose offer conforming to the solicitation will be most advantageous to the Government, price and other factors considered.

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New
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Solicitation # 75F40126R00009
Solicitation 75F40126R00009 is a request for proposals for a single Indefinite Delivery, Indefinite Quantity (IDIQ) contract to provide Contractor-Hosted Fully Integrated Records Facility (FIRF) services for the FDA. This acquisition is exclusively set aside for Service-Disabled Veteran-Owned Small Business (SDVOSB) concerns under NAICS code 541611. The contract has a maximum ceiling of 50 million dollars with a guaranteed minimum of 10,000 dollars. The anticipated period of performance consists of five 12-month ordering periods from December 1, 2026, through November 30, 2031, with an additional six-month option to extend services through May 31, 2032. The contract will support various task order types, including Time-and-Materials, Labor-Hour, and Firm-Fixed Price. The scope of work requires the contractor to manage an offsite document control facility to standardize records management and transition the agency toward a near 100 percent electronic environment for premarket and postmarket submissions. Key task areas include program management, document processing, scanning, data entry, tracking, temporary storage, and transition activities. Performance will primarily occur at FDA facilities in the Washington, D.C. metropolitan area, specifically within Maryland. Award will be made on a Lowest Price-Technically Acceptable (LPTA) basis, evaluating technical factors and past performance on an acceptable or unacceptable basis. Proposals must be submitted electronically in three separate volumes, with a final submission deadline of November 5, 2026, at 2:00 PM Eastern Time.
Administrative Management and General Management Consulting Services

POSTED

2 days ago

DEADLINE

in 7 days
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