Request for Information (RFI): Commercial Off-the-Shelf Task Management Tool

Closed Special Notice Posted

Solicitation number
FDA-RFI-2026-032726
Agency
Responses due
Set-aside
No set-aside

Opportunity facts

Place of performance
Maryland, United States

Notice details come from SAM.gov. Updated .

About this opportunity

The Food and Drug Administration (FDA), operating under the Department of Health and Human Services, issued Request for Information (RFI) FDA-RFI-2026-032726 on March 12, 2026, to gather market intelligence on Commercial Off-the-Shelf (COTS) task management tool solutions. This is a purely informational market research initiative under FAR Part 10 and does not constitute a binding solicitation or commitment to award a contract. The RFI seeks vendor information regarding solutions capable of supporting the FDA Executive Secretariat's correspondence and task management operations. Responses are voluntary and become government property, with all associated response costs borne by vendors. The FDA explicitly will not accept unsolicited proposals in response to this notice. Amendment 1, issued on March 26, 2026, extended the response deadline and clarified pricing submission requirements.

The FDA seeks comprehensive task management solutions to support approximately 16,000 federal staff with capabilities including correspondence intake, multi-office document clearance workflows, deadline tracking with escalation alerts, collaboration features, and regulatory-compliant audit trails. Vendors must submit responses by 5:00 PM EST on April 3, 2026, to Lilibeth Deato at lilibeth.deato@fda.hhs.gov, providing executive summaries, detailed capability descriptions, security certifications (FedRAMP, FISMA, NIST compliance), integration specifications, cost estimates for a five-year period with tiered pricing structures, and past performance from at least three comparable federal deployments. The solution must scale from an initial FDA deployment of 16,000 users to potential HHS enterprise expansion supporting 50,000 users, with flexible licensing models for viewers, creators, and administrators. Key requirements include FDA Title 21 CFR Part 11 digital signature capabilities, CAC/PIV card integration, and NARA records management compliance. There are no set-aside requirements or specific eligibility restrictions; any vendor with relevant COTS solutions may submit a response.

Notice text

2 versions

Update #2 · Latest ·

03/26/2026 Please review the attached document (Amendment 1).

The purpose of this Request for Information (RFI) is to obtain technical and business information from the marketplace regarding the availability of Commercial Off-the-Shelf (COTS) solutions capable of supporting the U.S. Food and Drug Administration (FDA) Executive Secretariat's correspondence and task management requirements.

Update #1 ·

The purpose of this Request for Information (RFI) is to obtain technical and business information from the marketplace regarding the availability of Commercial Off-the-Shelf (COTS) solutions capable of supporting the U.S. Food and Drug Administration (FDA) Executive Secretariat's correspondence and task management requirements.

Files

File Type Posted
Amendment 1.pdf PDF
TMT RFI HHS Versionv2.pdf PDF
FDA Task Management Vendor Response Templatev2.xlsx XLSX spreadsheet

Similar open opportunities

Opportunity Agency Set-aside Responses due
Contractor-Hosted Fully Integrated Records Facility (FIRF) IDIQ Silver Spring, Maryland 20993, United States · NAICS 541611 FDA Office of Acquisition and Grant Services Service-Disabled Veteran-Owned Small Business

On GovTribe

Work this opportunity

  • Track it in your pipeline
  • Find teaming partners
  • Similar opportunities
  • Ask GovTribe AI about this opportunity