Request for Information (RFI): Commercial Off-the-Shelf Task Management Tool V2
Overview
Buyer
Place of Performance
NAICS
PSC
Set Aside
Original Source
Timeline
Qualification Details
Fit reasons
- NAICS alignment with historical contract wins in similar service areas.
- Scope strongly matches core technical capabilities and delivery model.
Risks
- Past performance thresholds may require one additional teaming partner.
- Potential clarification needed on staffing minimums before bid/no-bid.
Next steps
Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.
Quick Summary
The U.S. Food and Drug Administration (FDA) has issued a Request for Information (RFI) for Commercial Off-the-Shelf (COTS) Task Management Tool V2. This RFI seeks technical and business information from the marketplace regarding solutions capable of supporting the FDA Executive Secretariat's correspondence and task management requirements. Responses are due by March 27, 2026, at 5 PM EST.
Purpose & Scope
This RFI is for market research purposes only and does not constitute a solicitation. The FDA aims to identify potential vendors offering comprehensive COTS solutions for executive correspondence workflows, document clearance processes, inter-agency coordination, task tracking, and workflow automation. The solution should manage high-volume, time-sensitive correspondence, ensure statutory deadline compliance, and provide comprehensive audit trails.
Key Requirements
The FDA is interested in solutions that offer:
- Comprehensive enterprise Task Management Tools, including licensing, support, and documentation.
- Effective task management capabilities with minimum effort and cost.
- Scalability, security, and seamless integration with federal systems (e.g., SharePoint, Teams, Outlook).
- Document clearance and approval workflows (sequential and parallel routing, comment management, version control, digital signatures).
- Compliance with federal security and records management standards (e.g., FedRAMP, FISMA, NIST, NARA, Title 21 CFR Part 11).
- Scalability to support up to 16,000 personnel initially, with potential for HHS enterprise deployment up to 50,000 personnel.
- Analysis of Total Cost of Ownership (TCO).
Submission Details
- Responses Due: March 27, 2026, by 5 PM EST.
- Submission Method: Email to
lilibeth.deato@fda.hhs.gov. - Subject Line:
FDA-RFI-2026-032726 - Commercial Off-the-Shelf (COTS) Task Management Tool (TMT). - Page Limit: Not to exceed 8 pages of text (graphics, tables, diagrams, and spreadsheets do not count).
- Format: Times New Roman, 12-point font, 8.5 x 11-inch paper, 0.5" margins.
- Cover Page: Must include company name, service line, CAGE code, UEI, address, Point of Contact, business size, small business status, and GWAC contract details if applicable.
- Vendor Response Template: Bidders must use the provided Excel template (
FDA Task Management Vendor Response Templatev2.xlsx) to detail pricing for software licenses, implementation, data migration, training, annual maintenance, professional services, and a 5-year Total Cost of Ownership (TCO) for both FDA and potential HHS enterprise expansion.
Contract & Timeline
- Type: Special Notice (Request for Information)
- Published: March 12, 2026
- Response Due: March 27, 2026
Set-Aside
None specified.
Additional Notes
This RFI is for information gathering only; submissions are voluntary and become government property. Proprietary, classified, or sensitive information should not be included. The FDA will not acknowledge receipt or notify respondents of the outcome. No phone calls will be accepted.