2 PAM Autoinjectors
ID: 2-PAM-BARDAType: Sources Sought
Overview

Buyer

HEALTH AND HUMAN SERVICES, DEPARTMENT OFOFFICE OF ASSISTANT SECRETARY FOR PREPAREDNESS AND RESPONSEBARDA - ASPR / DAAPPO / BARDA DCMAWASHINGTON, DC, 20515, USA

NAICS

Research and Development in Biotechnology (except Nanobiotechnology) (541714)
Timeline
    Description

    The Department of Health and Human Services, specifically the Biomedical Advanced Research and Development Authority (BARDA), is seeking market information regarding the development and manufacturing of 2-PAM (Pralidoxime) autoinjectors intended for the treatment of organophosphate poisoning, including exposure to nerve agents. The objective is to gather data on the capabilities of businesses to produce FDA-approved autoinjectors, with a requirement to manufacture up to 2 million units that meet Emergency Use Authorization standards by 2027. This initiative is crucial for ensuring effective public health responses to chemical, biological, radiological, and nuclear (CBRN) threats through adequate medical countermeasures. Interested parties must submit their responses, including business and technical representations, by May 14, 2025, and can contact Kevin Dean at kevin.dean1@hhs.gov or Erin Greninger at erin.greninger@hhs.gov for further information.

    Point(s) of Contact
    Kevin Dean, Contracting Specialist
    (202) 989-5371
    kevin.dean1@hhs.gov
    Erin Greninger, Contracting Officer
    (771) 210-7767
    erin.greninger@hhs.gov
    Files
    Title
    Posted
    The Sources Sought Notice (SSN No. 2-PAM-BARDA) is issued by the Biomedical Advanced Research and Development Authority (BARDA) to collect information on the market capabilities for developing and manufacturing 2-PAM (Pralidoxime) autoinjectors intended for the treatment of organophosphate poisoning, including exposure to nerve agents. This notice is for market research purposes only and does not constitute a contract award. BARDA seeks input from both small and other than small business entities regarding their capacity to produce FDA-approved autoinjectors capable of fulfilling Emergency Use Authorization standards by 2027. Key requirements include the ability to manufacture 2 million units and meeting FDA reliability standards. The notice details specific guidelines for submitting business and technical representations, emphasizing the necessary qualifications, prior experience, and technical capabilities. Responses are required by May 14, 2025, and include important regulatory information concerning ongoing development and manufacturing capabilities. Overall, this SSN aims to enrich BARDA's planning for potential acquisitions while ensuring effective public health responses to CBRN threats through adequate medical countermeasures.
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    Title
    Type
    2 PAM Autoinjectors
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