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65 -- OraQuick Rapid HIV Test Kits and Test Kit Controls

Active
N00033-04-Q-9029Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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Military Sealift Command plans to award a sole-source contract to OraSure Technologies, Inc. for the procurement of approximately 6,000 HIV-1 rapid test kits along with 240 Test Control Kits, which are essential for quality control during testing. These rapid test kits are a key element in the prescreening process for the smallpox immunization program, requiring an FDA-approved, CLIA-waived point-of-care finger-stick test that delivers immediate results. The test must be highly sensitive and specific to ensure accuracy in field conditions. The contract, identified under solicitation number N00033-04-Q-9029, is managed by the Military Sealift Command, part of the Department of Defense, and is headquartered in Norfolk, Virginia. The acquisition emphasizes the need for reliable and quick diagnostic tools to support military health initiatives. Key contacts for the contract include Brian HJ Kimm and Contract Specialist Kevin M Spillane, both reachable via their Navy email addresses and phone numbers. This procurement reflects the importance of maintaining effective and efficient medical readiness for military personnel.

General Info

Military Sealift Command awards OraSure Technologies a sole-source contract for 6,000 HIV-1 rapid test kits.

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

VA

Set-Aside

NONE

Documents

0

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Timeline

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special-notice

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Organization & Contact Information

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AgencyDepartment Of Defense → Military Sealift Command
Contacts2 people available
OfficeNORFOLK, VA, 23511-2419, USA
Office AddressNORFOLK, VA, 23511-2419, USA
Contacts
Kevin M SpillaneContract Specialist

Full Description

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Military Sealift Command intends to issue a sole-source award to OraSure Technologies, Inc. for an estimated 6,000 HIV-1 rapid test kits and an estimated 240 Test Control Kits (quality control reagents required to be run under several circumstances, including whenever a new lot of the test is used for the first time). The test kit is a critical component of the prescreening portion of the smallpox immunization program. The test kit must be a rapid point-of-care finger-stick FDA approved field test with CLIA waiver that is extremely sensitive and specific. Results must be immediately available. *Numbered note 22 applies.

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