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.

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Technical Documentation & Compliance Support Provider

Closed

Federal

Submission Closed06/01/2026, 07:00:00 PM UTC

Contract Overview

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

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NAICS: 541690

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RFQ6082 Noise Compliance & Air Quality Testing Services

Solicitation # RFQ6082

Management & Training Corporation (MTC) is soliciting bids for industrial hygienist services to conduct noise compliance and air quality testing at the San Diego Job Corps Center in Imperial Beach, California. The scope of work involves full-day monitoring and reporting from 7:00 am to 4:00 pm, specifically targeting Building 13 hard-trades shops and Building 225A welding shop. The selected contractor must perform a noise compliance audit based on OSHA 29 CFR 1910.95 and ANSI standards, as well as air quality assessments for particulate matter, welding fumes, VOCs, combustion gases, and ventilation performance in accordance with OSHA, ACGIH, and EPA standards. Deliverables include comprehensive Noise Compliance and Air Quality Compliance reports submitted in PDF format via email. This is a fee-for-service subcontracting opportunity under NAICS code 541690, open to various small business set-asides including SDB, WOSB, HUBZone, VOSB, and SDVOSB. Bidders must submit a lump sum fee via a bid sheet, along with a completed supplier packet containing a W-9, self-certification form, and proof of insurance by September 16, 2026, at 3:00 PM PST. The contract requires adherence to Service Contract Labor Standards and prevailing wage determinations for San Diego County. Award selection will be based on the best value as determined by MTC. Contractors must also comply with federal regulations regarding the protection of sensitive information and the Buy American Act.

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AI Contract Overview

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 SvcsView Agency

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Set-Aside

NONE

Documents

This scope was carved out of 75F40126SSN133239.

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

View the prime solicitation

FDA - SubCutaneous Injection Site Simulator

AI Contract Breakdown

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Timeline

PhaseClosed

PostedMay 27

subcontract

Response DeadlineJun 1

Deadline has passed

Submission Closed

06/01/2026, 07:00:00 PM UTC

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Organization & Contact Information

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

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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