Medical Laboratory Services
ID: 75F40125Q129235Type: Combined Synopsis/Solicitation
Overview

Buyer

HEALTH AND HUMAN SERVICES, DEPARTMENT OFFOOD AND DRUG ADMINISTRATIONFDA OFFICE OF ACQ GRANT SVCSBeltsville, MD, 20705, USA

NAICS

Medical Laboratories (621511)

PSC

MEDICAL- LABORATORY TESTING (Q301)
Timeline
    Description

    The Department of Health and Human Services, specifically the Food and Drug Administration (FDA), is seeking proposals for medical laboratory services at the National Center for Toxicological Research (NCTR) in Jefferson, Arkansas. The procurement aims to establish a reliable service for on-site phlebotomy and various laboratory analyses necessary for employee medical surveillance, particularly for those exposed to hazardous materials or animals, ensuring compliance with Clinical Laboratory Improvement Amendments (CLIA) standards and HIPAA guidelines. This contract is crucial for maintaining employee health and safety while adhering to federal regulations regarding laboratory standards. Proposals are due by the specified deadline, with the contract expected to commence on July 30, 2025, and options for extensions through 2030. Interested parties can contact Howard Nesmith at howard.nesmith@fda.hhs.gov or call 870-543-7459 for further information.

    Point(s) of Contact
    Files
    Title
    Posted
    The document outlines a combined synopsis and solicitation from the Food and Drug Administration (FDA) for medical laboratory services at the National Center for Toxicological Research (NCTR) in Jefferson, Arkansas. The Request for Quote (RFQ) is intended for unrestricted competition, inviting proposals for on-site phlebotomy and various laboratory analyses required for employee medical surveillance, particularly for those exposed to hazardous materials or animals. Key services include routine blood chemistries, chest X-rays, and additional tests based on physician orders. Contractors must ensure compliance with Clinical Laboratory Improvement Amendments (CLIA) standards, provide timely reporting of lab results, and adhere to HIPAA guidelines. The contract will start on July 30, 2025, with options for extensions through 2030. Proposals must detail compliance with performance requirements, demonstrate technical capabilities, and provide competitive pricing. The overarching purpose of the solicitation is to establish a reliable service for medical monitoring within the FDA, ensuring employee safety and health while maintaining adherence to federal regulations regarding laboratory standards and employee welfare.
    Lifecycle
    Title
    Type
    Combined Synopsis/Solicitation
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