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This Sources Sought opportunity from Department Of Health And Human Services was posted on December 26, 2024. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Request for Information (RFI): OII-Extended Reality/Reality Simulation Training & Development Capability

Closed
RFQ1736621Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

General Info

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

NAICS

N/A

Place of Performance

MD, 20903, USA

Set-Aside

NONE

Documents

1

FDA OII - Extended Reality/Reality Simulation Training RFI

DOCX, Low priority6 pages · rfi
Low

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Timeline

1 update
PhaseClosed
Posted

Sources Sought

Deadline changed

Response deadline changed from Jan 2, 2025 to Jan 17, 2025.

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Contacts1 person available
OfficeBeltsville, MD, 20705, USA
Organization / AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Office AddressBeltsville, MD, 20705, USA
Contacts
Vivianna Diaz
contact@example.gov

Full Description

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This Request for Information (RFI) is being issued by the Food and Drug Administration (FDA) in accordance with Federal Acquisition Regulations (FAR) Part 10, Market Research. It is for information, planning and market research purposes only and shall not be construed as either a solicitation or obligation on the part of the FDA or its Centers. The purpose of this RFI is to broaden FDA's understanding of current market capability on Artificial Intelligence-powered Extended Reality (XR) reality simulation tools such as Augmented Reality (AR) or Virtual Application (VR) training platforms to provide the next generation immersive learning, experiential learning, and microlearning opportunities for FDA regulatory inspection/investigation workforce. Responses are to be submitted to Vivianna Diaz, Vivianna.diaz@fda.hhs.gov , Contract Specialist. Email is preferred. Please include the RFI number in the response. Do not send information that requires a non-disclosure agreement or sensitive business information. Telephone inquiries will not be accepted or acknowledged, and no feedback or evaluations will be provided to companies regarding their submissions. Interested companies must submit a Capability Statement limited to 10 pages that provides responses to the following requested information. Capability statements will not be returned and will not be accepted after the due date.

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