Request for Information (RFI) Application Programing Interface (API) Enterprise Management Solutions
ID: FDA-RFI-75F40125Q00052Type: Sources Sought
Overview

Buyer

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

    The Department of Health and Human Services, through the Food and Drug Administration (FDA), is seeking information regarding Application Programming Interface (API) Enterprise Management Solutions to support its enterprise-wide API strategy. The primary objective of this Request for Information (RFI) is to gather insights on existing or potential solutions that can standardize and streamline the management of APIs currently dispersed throughout the organization, with a focus on scalability, security, and total cost of ownership. This initiative is crucial for modernizing legacy systems and enhancing operational efficiency within the FDA. Interested vendors are encouraged to submit their responses by December 20, 2024, and can direct inquiries to Noah Padilla at Noah.Padilla@fda.hhs.gov.

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    Title
    Posted
    The FDA's Request for Information (RFI) no. FDA-RFI-75F40125Q00052 aims to gather market insights on potential Application Programming Interface (API) Enterprise Management Solutions to support its enterprise-wide API strategy. The RFI emphasizes the FDA's need for a unified API management platform to standardize and streamline licensing, management, and migration of existing APIs, currently scattered across the organization. Key objectives include identifying qualified vendors, evaluating API scalability and security, and assessing the total cost of ownership. The document outlines expected capabilities, such as multi-cloud integration, API governance, and real-time data services, with a focus on modernizing legacy systems and enhancing operational efficiency. Vendors are requested to provide comprehensive information regarding their offerings, pricing models, and migration support, along with case studies and compliance with relevant security standards. The submission deadline is set for December 20, 2024, with specific guidelines for presenting responses. The RFI is a preliminary step in FDA's market research and does not commit to any contract award or selection process based on submissions.
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