This Combined Synopsis/Solicitation opportunity from Department Of Health And Human Services was posted on July 28, 2025. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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Do Laboratory Prescribed and Ad Libitum Use Sessions Represent Real-World ENDS Use?

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75F40125R00096Federal

Submission Closed08/25/2025, 06:00:00 PM UTC

Contract Overview

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

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NAICS: 541380

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Navsup Weapon Systems Support

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Navsup Weapon Systems Support Mech

POSTED

about 7 hours ago

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in about 1 month

AI Contract Overview

The contract pertains to a research project conducted by the Food and Drug Administration (FDA) to evaluate whether laboratory-prescribed and ad libitum use sessions accurately reflect real-world electronic nicotine delivery systems (ENDS) usage patterns. The solicitation, identified as 75F40125R00096, was posted on July 28, 2025, with a response deadline of August 25, 2025. The project is a combined solicitation with no specific set-aside restrictions, indicating it is open to all qualified entities. The work will be performed primarily in Rockville, Maryland, and involves analyzing the behaviors associated with ENDS use to inform regulatory decisions and public health policies. Key contacts for the project include Janice Heard and Madeline Bryant from the FDA, who can be reached via email or phone for further inquiries. The contract emphasizes understanding the differences between controlled laboratory sessions and real-world usage, which is critical for assessing the health impacts and regulatory considerations of ENDS products. The opportunity is publicly accessible through the SAM.gov portal, providing detailed information for interested parties to submit proposals.