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Preclinical and Clinical Research Support 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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This subcontract for Preclinical and Clinical Research Support Services involves providing specialized research and trial execution for prime contractors on CPE CBRND projects. The scope of work includes conducting efficacy pharmacology and toxicology studies, managing human clinical trials, and employing computational or biological modeling to predict the efficacy of countermeasures. The selected provider must possess GLP certification and demonstrate expertise in FDA regulatory submissions. Key deliverables for this Department of Defense project include detailed efficacy reports, comprehensive toxicology data, and completed regulatory submission packages.

General Info

GLP-certified provider delivers preclinical and clinical research support for DoD CBRND projects.

Agency

Department Of Defense → W6QK Acc-ApgView Agency

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)View NAICS

Place of Performance

MD

Set-Aside

NONE

Documents

This scope was carved out of W911SR-26-R-HEAL.

The full solicitation package (3 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

Chemical, Biological, Radiological, and Nuclear (CBRN) Medical Countermeasure (MCM) Participant Basic Agreement (PBA)

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Timeline

PostedAug 19

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Organization & Contact Information

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AgencyDepartment Of Defense → W6QK Acc-Apg

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Defense → W6QK Acc-Apg

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Office AddressN/A

ContactsNo contact information available

Full Description

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Performs specialized research and trial execution for prime contractors on CPE CBRND projects. Conducts efficacy pharmacology and toxicology studies, manages human clinical trials, and utilizes computational or biological modeling to predict countermeasure efficacy. Requires GLP certification and FDA regulatory submission expertise. Delivers efficacy reports, toxicology data, and regulatory submission packages.

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