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Sirce II

ID: 75F40126Q00072 • Type: Sources Sought • Match:  95%
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Description

Posted: Feb. 24, 2026, 1:48 p.m. EST

The purpose of Amendment 03 is to increase the page limit to 10 pages.

The purpose of Amendment 02 is to remove this statement formerly located in the last paragraph, " Please note that a respondent's failure to provide a complete response to the information requested in this Section 7, will be interpreted to mean that it does not understand what information is being requested and does not demonstrate the capability to provide services required."

The purpose of Amendment 01 is to correct the estimated ceiling from $400,000,000 to $300,000,000.

The U.S. Food and Drug Administration (FDA) is conducting market research to identify qualified vendors capable of supporting the OII Systems for Inspection & Imports, Recalls Compliance, and Enforcement (SIRCE) II initiative. This Request for Information (RFI) is issued solely for market research purposes to assess industry capabilities, capacity, and innovative approaches for delivering comprehensive IT modernization and support services.

Posted: Feb. 23, 2026, 2:04 p.m. EST
Posted: Feb. 23, 2026, 10:42 a.m. EST
Posted: Feb. 19, 2026, 9:28 a.m. EST
Background
The U.S. Food and Drug Administration (FDA) is conducting market research to identify qualified vendors capable of supporting the OII Systems for Inspection & Imports, Recalls Compliance, and Enforcement (SIRCE) II initiative. This Request for Information (RFI) is issued solely for market research purposes to assess industry capabilities, capacity, and innovative approaches for delivering comprehensive IT modernization and support services. The goal of this initiative is to leverage effective industry capabilities and innovative approaches available in the marketplace.

Work Details
The FDA aims to gather input on its draft critical Statement of Work (SOW) Task Areas and Technology Stack. The objectives include:

1. Assessing Market Capabilities: Evaluate industry capacity to meet technical and operational requirements.

2. Gathering Industry Feedback: Collect recommendations for improving solicitation approach, evaluation criteria, and technical requirements.

3. Understanding Pricing Approaches: Gain insights into cost structures and performance optimization strategies.

4. Identifying Innovation Opportunities: Explore emerging technologies and best practices that could enhance program outcomes.

The SOW includes critical task areas such as Systems Integration and Engineering Services, which involve developing integration strategies for evolving systems, phasing out legacy systems, and collaborating with other organizations; Architecture Support Services aimed at minimizing development costs while enhancing IT capabilities; and Artificial Intelligence support services focused on integrating AI technologies to enhance regulatory mission capabilities.

Overview

Response Deadline
March 6, 2026, 12:00 p.m. EST Past Due
Posted
Feb. 19, 2026, 9:28 a.m. EST (updated: Feb. 24, 2026, 1:48 p.m. EST)
Set Aside
None
Place of Performance
Rockville, MD United States
Source

Current SBA Size Standard
$34 Million
Pricing
Multiple Types Common
Est. Level of Competition
Low
Odds of Award
29%
On 2/19/26 Food and Drug Administration issued Sources Sought 75F40126Q00072 for Sirce II due 3/6/26. The opportunity was issued full & open with NAICS 541512 and PSC DA01.
Primary Contact
Name
Noah Padilla   Profile
Phone
None

Secondary Contact

Name
Steven Gagnon   Profile
Phone
None

Documents

Posted documents for Sources Sought 75F40126Q00072

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Additional Details

Source Agency Hierarchy
HEALTH AND HUMAN SERVICES, DEPARTMENT OF > FOOD AND DRUG ADMINISTRATION > FDA OFFICE OF ACQ GRANT SVCS
FPDS Organization Code
7524-00223
Source Organization Code
100188033
Last Updated
March 21, 2026
Last Updated By
noah.padilla@fda.hhs.gov
Archive Date
March 21, 2026