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This Government Contract opportunity from Department Of Defense was posted on May 26, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

FDA Regulatory & Compliance Support

Closed
Federal

Contract Overview

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This subcontract, titled "FDA Regulatory & Compliance Support," involves providing specialized regulatory consulting services to ensure continuous compliance with FDA requirements related to the use of Implantable Contact Lenses (ICL). The scope includes managing adverse event reporting, ensuring accurate labeling, and conducting thorough post-market surveillance to meet all necessary regulatory standards. The contract is issued by the Department of Defense through the W40M MRC0 West agency and is performed at Fort Hood, with a postal code of 76544. The solicitation was posted on May 26, 2026, with a response deadline set for June 4, 2026, at 3:00 PM. Classified as a subcontract under NAICS code 541690, which covers other scientific and technical consulting services, it does not specify any particular set-aside or organization type. This opportunity is aimed at securing expertise to maintain FDA compliance and support ongoing regulatory obligations connected with the ICL product lifecycle.

General Info

Provide FDA regulatory consulting for Implantable Contact Lenses, including reporting, labeling, and surveillance.

Agency

Department Of Defense → W40M MRC0 West

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Fort Hood, TX, 76544, USA

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → W40M MRC0 West
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → W40M MRC0 West
Office AddressN/A
ContactsNo contact information available

Full Description

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Provide regulatory consulting to ensure ongoing compliance with FDA requirements for ICL use, including adverse event reporting, labeling, and post-market surveillance.