This Sources Sought opportunity from Department Of Health And Human Services was posted on November 20, 2023. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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Pharmacokinetic Analysis Resource Center

Closed

75N95024R00007SBFederal

Submission Closed12/11/2023, 06:00:00 PM UTC

Contract Overview

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

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NAICS: 541715

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Solicitation # DARPA-PS-26-141

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Defense Advanced Research Projects Agcy

POSTED

1 day ago

DEADLINE

in about 2 months

General Info

Agency

Department Of Health And Human Services → National Institutes Of Health Nida

NAICS

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

Place of Performance

Bethesda, MD, 20892, USA

Set-Aside

SBA

Documents

Sources Sought Notice: Pharmacokinetic Analysis Resource Center (75N95024R00007SB)

sources-sought

Low

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Uniform Contract Format

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Timeline

PhaseClosed

PostedNov 20

Sources Sought

Response DeadlineDec 11

Deadline has passed

Submission Closed

12/11/2023, 06:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Health And Human Services → National Institutes Of Health Nida

Contacts2 people available

OfficeBethesda, MD, 20892, USA

Organization / AgencyDepartment Of Health And Human Services → National Institutes Of Health Nida

Office AddressBethesda, MD, 20892, USA

Contacts

Joshua T. Lazarus

Andrew Varley

Full Description

The Government is seeking Capability Statements on behalf of The National Institute on Drug Abuse (NIDA) Department of Therapeutics and Medical Consequences (DTMC) from Small Business organizations under the North American Industry Classification System (NAICS) code 541715, that can provide pharmacokinetic (PK) and pharmacodynamics (PD) aspects of the medications development. No actual clinical or laboratory studies will be carried out under this contract. The Contractor shall prepare study protocols, monitor clinical studies to assure that pertinent FDA regulations are met, perform data management and process clinical and pharmacokentic data, conduct PK, PD, and statistical analyses, and prepare study reports. The data/reports will be submitted to the FDA in support of IND's (Investigational New Drugs) and NDA's (New Drug Applicants).