Maryland Bids > Bid Detail

Opiate Immunoassay Test Reagent

Agency: DEPT OF DEFENSE
Level of Government: Federal
Category:
  • 65 - Medical, Dental, and Veterinary Equipment and Supplies
Opps ID: NBD00159252382402200
Posted Date: Nov 16, 2022
Due Date: Nov 21, 2022
Solicitation No: N6264523R0005
Source: https://sam.gov/opp/f7eeb416cb...
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Opiate Immunoassay Test Reagent
Active
Contract Opportunity
Notice ID
N6264523R0005
Related Notice
Department/Ind. Agency
DEPT OF DEFENSE
Sub-tier
DEPT OF THE NAVY
Major Command
NAVSUP
Sub Command
NAVSUP OTHER HCA
Sub Command 2
BUMED
Sub Command 3
NAVY MEDICINE SUPPORT COMMAND
Office
NAVAL MEDICAL LOGISTICS COMMAND
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General Information
  • Contract Opportunity Type: Solicitation (Updated)
  • All Dates/Times are: (UTC-05:00) EASTERN STANDARD TIME, NEW YORK, USA
  • Updated Published Date: Nov 16, 2022 11:50 am EST
  • Original Published Date: Oct 30, 2022 01:43 am EDT
  • Updated Date Offers Due: Nov 21, 2022 11:00 am EST
  • Original Date Offers Due: Nov 14, 2022 11:00 am EST
  • Inactive Policy: 15 days after date offers due
  • Updated Inactive Date: Dec 06, 2022
  • Original Inactive Date: Nov 29, 2022
  • Initiative:
    • None
Classification
  • Original Set Aside:
  • Product Service Code: 6550 - IN VITRO DIAGNOSTIC SUBSTANCES, REAGENTS, TEST KITS AND SETS
  • NAICS Code:
    • 325413 - In-Vitro Diagnostic Substance Manufacturing
  • Place of Performance:
    Frederick , MD 21702
    USA
Description

The Department of Defense (DOD) Drug Demand Reduction Program (DDRP) has a requirement for FDA and Quality management Documented Opiate immunoassay reagent kits for use with the currently installed Beckman Coulter AU5800 series systems. The reagents shall be capable of detecting of hydrocodone, hydromorphone, codeine, and morphine in human urine samples. Proposals shall comply with the Statement of Work (SOW).



The reagent kits are required for a period of performance of up to five (5) years. The estimated number of tests shall accommodate up to 500,000 tests per month.



The vendor shall comply with the FDA and Quality Management Documentation as specified in the SOW. The vendor shall comply with the Reagent Preparation and Calibration Information as specified in the SOW.



NOTE: The action previously designated as N6264522R0026 in FY22 has been replaced by this effort N6264523R0005 in FY23.



NOTE: Due to system issues, drafts of the SF-30 Amendment P00001 and a Conform SF-1449 are being attached as stopgap documents. As soon as the official SF-30 is generated these will be replaced.



Corrected documents are expected by 11-11-2022.


Attachments/Links
Contact Information
Contracting Office Address
  • 693 NEIMAN STREET
  • FORT DETRICK , MD 21702-9203
  • USA
Primary Point of Contact
Secondary Point of Contact


History

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