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This Government Contract opportunity from Department Of Defense was posted on May 15, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Content Review and Quality Assurance (QA) for SPL

Closed
Federal

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This contract involves the independent review and validation of Structured Product Labeling (SPL) content to ensure its accuracy, consistency, and compliance with FDA and government standards. The scope includes detailed verification of clinical pharmacology information, warnings, dosage instructions, and adverse reaction data to uphold regulatory requirements. The subcontract is managed by the Army Medical Resources Acquisition Activity under the Department of Defense and is set to be performed in Frederick, Maryland. The opportunity, titled "Regulatory Content Review and Quality Assurance (QA) for SPL," was posted on May 15, 2026, with a response deadline of June 5, 2026. It falls under the NAICS code 541611, indicating professional, scientific, and technical services. This contract seeks specialized expertise to conduct meticulous quality assurance of medical and regulatory content, supporting compliance efforts vital to public health and safety within the defense medical sector.

General Info

Independent review of SPL content for FDA compliance by Army Medical Resources Acquisition Activity.

Agency

Department Of Defense → Army Medical Resources Acq Activity

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

Frederick, MD, 21702, 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 → Army Medical Resources Acq Activity
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → Army Medical Resources Acq Activity
Office AddressN/A
ContactsNo contact information available

Full Description

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Independent review and validation of SPL content to ensure accuracy, consistency, and compliance with FDA and government requirements, including verification of clinical pharmacology, warnings, dosage, and adverse reactions.