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This Government Contract opportunity from Department Of Health And Human Services was posted on May 27, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Technical Documentation & Compliance Support Provider

Closed
Federal

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This contract involves the preparation and delivery of regulatory-compliant technical documentation essential for medical device submissions. The scope includes creating user manuals, safety data sheets (SDS), and compliance certificates, ensuring all materials meet the necessary regulatory standards. It is issued as a subcontract under NAICS code 541690, which pertains to specialized professional and technical services. The contract is managed by the FDA Office of Acquisition and Grant Services within the Department of Health and Human Services. The solicitation was posted on May 27, 2026, with a response deadline on June 1, 2026, at 7:00 PM. While specific location and contact details are not provided, the work supports the regulatory submission process for medical devices, underscoring the critical role of documentation in facilitating compliance and market approval.

General Info

Preparation and delivery of regulatory-compliant medical device documentation under subcontract NAICS 541690.

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

MD

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 Health And Human Services → FDA Office Of Acq Grant Svcs
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Health And Human Services → FDA Office Of Acq Grant Svcs
Office AddressN/A
ContactsNo contact information available

Full Description

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Development of regulatory-compliant technical documentation, including user manuals, safety data sheets (SDS), and compliance certificates for medical device submission.