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Human or Animal Subjects Research Support

Active
Federal

Contract Overview

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

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This subcontract for the Advanced Research Projects Agency for Health (ARPA-H) involves providing biological testing support for prime contractors through the execution of in-vivo or in-vitro studies. The selected provider will be responsible for managing subject protocols and delivering validated experimental data along with comprehensive clinical or pre-clinical reports. To qualify, the contractor must utilize facilities approved by the IRB or IACUC, and all key personnel are required to complete mandatory Human Subjects Research or Animal Subjects Research training. This opportunity, categorized under NAICS code 115210, has a response deadline of February 10, 2027.

General Info

Subcontract for ARPA-H biological testing support; deadline February 10, 2027; requires certified facilities.

Agency

Department Of Health And Human Services → Advanced Research Projects Agency For Health (arpa-H)View Agency

NAICS

115210 - Support Activities for Animal ProductionView NAICS

Place of Performance

DC, 20003, USA

Set-Aside

NONE

Documents

This scope was carved out of ARPA-H-SOL-26-150.

The full solicitation package (9 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

ARPA-H Emerging Health Innovators (EHI) Initiative

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → Advanced Research Projects Agency For Health (arpa-H)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Health And Human Services → Advanced Research Projects Agency For Health (arpa-H)
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Office AddressN/A
ContactsNo contact information available

Full Description

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Performs biological testing involving human or animal subjects for prime contractors on ARPA-H projects. Conducts in-vivo or in-vitro studies and manages subject protocols. Requires IRB or IACUC approved facilities and mandatory Human Subjects Research (HSR) or Animal Subjects Research (ASR) training for all key personnel. Delivers validated experimental data and clinical or pre-clinical reports.

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