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Preclinical and IND-Enabling Study Execution

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Federal

Contract Overview

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The contract involves conducting Good Laboratory Practice (GLP)-compliant non-clinical studies, including toxicology, pharmacokinetics, and shelf-stability testing, to support FDA Investigational New Drug (IND) applications. This subcontract is issued by the Defense Advanced Research Projects Agency, part of the Department of Defense, under the NAICS code 541611, which relates to administrative and management consulting services. The work is focused on preclinical and IND-enabling study execution, with a proposal response deadline of June 24, 2026. The contract does not specify a particular location for performance or set-aside designations, indicating flexibility in these areas. This effort is critical in ensuring that necessary non-clinical data meet regulatory standards to advance therapeutic candidates through the drug development pipeline.

General Info

Conduct GLP-compliant non-clinical studies supporting FDA IND applications; proposal due June 24, 2026.

Agency

Department Of Defense → Defense Advanced Research Projects Agcy

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

VA

Set-Aside

NONE

Documents

(0)

No documents available

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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
Office AddressN/A
ContactsNo contact information available

Full Description

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Conduct GLP-compliant non-clinical studies including toxicology, pharmacokinetics, and shelf-stability testing to support FDA IND applications.

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