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.