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This Subcontract opportunity from Department Of Defense was posted on July 12, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Compliance and Safety Documentation Services

Closed
Federal

Contract Overview

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The contract seeks services for the preparation and submission of hazard warning labels, material safety data sheets, and regulatory documentation required for medical devices, with a specific requirement to coordinate with FDA product specialists prior to contract award. This subcontract, issued under the NAICS code 541690, is part of a broader effort by the Department of Defense through the Medical Supply Chain MD Surg FSF to ensure compliance with federal safety and regulatory standards. The work is to be performed at an FPO address with a ZIP code of 96672-4090, indicating operations may involve overseas or military logistics support. All proposals must be submitted by the deadline of July 20, 2026, following the posting of the solicitation on July 12, 2026, and the contractor is expected to manage the full lifecycle of regulatory documentation, including accurate labeling and alignment with U.S. medical device regulatory frameworks.

General Info

Prepare and submit regulatory docs for medical devices, coordinate with FDA, perform work at FPO 96672-4090, submit proposal by July 20, 2026.

NAICS

541690 - Other Scientific and Technical Consulting Services

Place of Performance

FPO, AP, 96672-4090, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-222N.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

FILTER, AIR, SPIROMETER

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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 → MEDICAL SUPPLY CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Preparation and submission of hazard warning labels, MSDS, and regulatory documentation for medical devices, including coordination with FDA product specialists prior to award.

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