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Policy and Regulatory Impact Research Support

Active

Federal

Response Deadline08/07/2026, 02:00:00 PM UTC

Contract Overview

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

AI Contract Overview

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The contract titled Policy and Regulatory Impact Research Support is a subcontract under the FDA Office of Acquisition Grant Services, part of the Department of Health and Human Services, aimed at translating complex data insights into actionable policy briefs, regulatory impact assessments, and decision support tools for FDA program offices. The work requires expertise in data analysis, regulatory science, and policy communication to produce clear, evidence-based outputs that inform FDA’s regulatory and operational decisions. The solicitation was posted on July 31, 2026, with a response deadline of August 7, 2026, and falls under NAICS code 923120, which corresponds to regulatory functions generally performed by government agencies. Performance location and specific office details are not provided, and no set-aside status or point of contact information is included, indicating a focus on technical capability rather than socioeconomic preferences. Interested parties must submit proposals before the deadline to support FDA’s mission of ensuring public health through science-informed regulation.

General Info

Support FDA with data-driven policy briefs and regulatory assessments through technical expertise by August 7, 2026.

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant SvcsView Agency

NAICS

923120 - Administration of Public Health ProgramsView NAICS

Place of Performance

MD

Set-Aside

NONE

Documents

(0)

No documents available

AI Contract Breakdown

Uniform Contract Format

No contract breakdown available.

Cannot generate Contract Breakdown because no documents were found from this contract's source.

Timeline

PostedJul 31

subcontract

Response DeadlineAug 7

Submission deadline

Response Deadline

08/07/2026, 02:00:00 PM UTCin 6 days

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Organization & Contact Information

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

ContactsNo contacts available

OfficeN/A

Organization / Agency

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

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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Translate data insights into policy briefs, regulatory impact assessments, and decision support tools for FDA program offices.

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Protective Clothing Blood Penetration Resistance Tester

Solicitation # 75F40126Q134448

The U.S. Food and Drug Administration’s Office of Acquisition and Grant Services, under the Department of Health and Human Services, is seeking a Protective Clothing Blood Penetration Resistance Tester through a combined synopsis and solicitation numbered 75F40126Q134448, posted on July 31, 2026, with responses due by August 7, 2026, at 6:00 PM Eastern Time. The procurement targets a specialized testing device designed to evaluate the resistance of protective clothing against blood penetration, critical for ensuring safety standards in medical and emergency response environments. The North American Industry Classification System code 334516 indicates the requirement falls under manufacturing instruments and related products. The place of performance is designated as Winchester, Massachusetts, with a zip code of 01890, while the contracting office is located in Rockville, Maryland, 20852. The sole point of contact for this solicitation is Warren Dutter, who can be reached via phone at 301-796-2486 or email at warren.dutter@fda.hhs.gov, and is responsible for overseeing all aspects of the procurement. No set-aside type is specified, meaning the contract is open to all eligible vendors without preference for small businesses, veteran-owned firms, or other categories. The solicitation is issued through SAM.gov, and potential offerors must access the detailed requirements via the provided UI link to review full technical specifications, evaluation criteria, and submission instructions. The equipment must meet exacting performance benchmarks to ensure compliance with federal safety protocols and interoperability with existing testing frameworks used by the agency.

Analytical Laboratory Instrument Manufacturing

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