Safe Medication Use
ID: FDA-RFI-126495Type: Sources Sought
Overview

Buyer

HEALTH AND HUMAN SERVICES, DEPARTMENT OFFOOD AND DRUG ADMINISTRATIONFDA CENTER FOR DRUG EVALUATION AND RESEARCHSilver Spring, MD, 20993, USA

NAICS

All Other Professional, Scientific, and Technical Services (541990)

Original Source

https://sam.gov/opp/9ae04c73a15f484e85d7546a1edef206/view
Timeline
    Description

    The U.S. Food and Drug Administration (FDA) is conducting a Request for Information (RFI) to identify potential sources capable of providing medication error reports, an analytics platform, and related services aimed at preventing and analyzing medication errors. This initiative, led by the FDA's Center for Drug Evaluation and Research, seeks organizations that can supply nationwide data from healthcare providers, consumers, and patient safety organizations, emphasizing the importance of robust reporting, data analysis, and training in enhancing medication safety protocols. Interested parties, particularly small businesses, are encouraged to submit their capability statements by January 6th, 2025, and should note that responses are voluntary and do not imply a commitment for a contract. For further inquiries, contact Brian Wodzisz at Brian.Wodzisz@fda.hhs.gov or call 301-796-7376.

    Point(s) of Contact
    Brian Wodzisz
    (301) 796-7376
    Brian.Wodzisz@fda.hhs.gov
    Files
    Title
    Posted
    RFI_SafeMedUse.pdf
    The FDA's Center for Drug Evaluation and Research (CDER) is seeking information through a Request for Information (RFI) to explore potential sources for medication error reports, an analytics platform, and related services aimed at preventing and analyzing medication errors. This initiative, driven by the Office of Surveillance and Epidemiology, targets organizations capable of providing nationwide data collected from healthcare providers, consumers, and patient safety organizations. The RFI emphasizes that responses are voluntary and do not imply a commitment for a contract. Vendors must demonstrate specific capabilities and provide detailed capability statements, showcasing their experience and insights on cost-effective solutions, risk mitigation, and resource requirements. The project's objectives include robust reporting, data analysis, and training, underpinned by the necessity for rigorous data management and responsiveness to public health concerns. The FDA encourages small businesses to participate and highlights its rights to utilize submitted non-proprietary data in future solicitations. Responses are due by January 6th, 2025, emphasizing the FDA's commitment to enhancing medication safety protocols through informed partnerships.
    Lifecycle
    Title
    Type
    Safe Medication Use
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