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Preclinical and GLP-Compliant Animal Testing Services

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Federal

Contract Overview

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

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The contract requires the execution of Good Laboratory Practice-compliant preclinical animal studies to assess the safety and efficacy of a novel biomedical technology, with the explicit purpose of supporting regulatory submission. All studies must adhere strictly to GLP standards to ensure data integrity, reproducibility, and acceptance by regulatory authorities. The work is part of a subcontract under the Department of Defense, specifically managed by the Defense Advanced Research Projects Agency, and is classified under NAICS code 541940 for scientific research and development services. The solicitation was posted on July 2, 2026, with a firm response deadline of July 29, 2026, indicating a tight timeline for prospective providers to submit proposals. Performance location details are not specified, but the scope demands specialized laboratory infrastructure and qualified personnel capable of conducting complex in vivo testing under controlled, regulated conditions. This effort supports a critical defense-related biomedical initiative, requiring high levels of technical precision, documentation rigor, and compliance with federal research protocols.

General Info

GLP-compliant preclinical animal studies for defense biomedical tech, due July 29, 2026.

Agency

Department Of Defense → Defense Advanced Research Projects AgcyView Agency

NAICS

541940 - Veterinary Services View NAICS

Place of Performance

VA

Set-Aside

NONE

Documents

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Advanced Research Projects Agcy
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → Defense Advanced Research Projects Agcy
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Office AddressN/A
ContactsNo contact information available

Full Description

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Conduct GLP-compliant preclinical animal studies to evaluate safety and efficacy of a novel biomedical technology for regulatory submission.

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