FOIA REDACTION (FRED) TOOL
Department of Health and Human Services · HHS/FDA/CDER
Overview
- Development stage
- DeployedSource: c) Deployed – The use case is being actively authorized or utilized to support the functions or mission of an agency.
- High-impact designation
- Presumed high-impact, determined notSource: b) Presumed high-impact, but determined not high impact
- Impact justification
- FRED should not be considered a high-impact AI use case because: a. It operates as a recommendation system only, with mandatory human review and approval required for all outputs. b. No automated decisions are made - humans retain full control over all redaction decisions. c. It serves as an assistive tool to improve efficiency while maintaining human oversight and accountability for all FOIA compliance decisions.
- Start date
- 2025-05 (month precision)Source: May-25
- Withheld from public reporting
- NoSource: a) No
Mission
- Topic area
- Health and Medical
- Operational functions
- FOIA and records management Derived by keyword rules; see methodology
Problem the AI is intended to solve
FRED is designed to support FOIA staff in redacting records more efficiently and consistently. FOIA redaction can be a time-consuming process and experience large back-logs of requested documents. It aims to use AI to analyze, identify, and generate predictions of text for redaction, thereby improving the efficiency of FOIA response processing.
Expected benefits
More efficient releases of documents in response to FOIA requests, reduction in back-logs, helping ensure public access to government information while protecting sensitive data appropriately.
System outputs
FRED produces a PDF with boxes around text that it recommends for redaction along with comments for the redaction code
Technology
- AI classification
- Generative AISource: Generative AI: AI that generates new or synthetic content (e.g., images, videos, audio, text, code).
- System name(s)
- Elsa
- Custom-developed code
- Yes
- Public source code
- Not reported
Sourcing
- How it was built
- Contract and in-houseSource: c) Developed with both contracting and in-house resources
- Vendor (as reported)
- Contractor teams
- Vendors (standardized)
- None on the standard list
A vendor is the supplier named by the agency. It does not identify the underlying model or AI technology.
Data and privacy
- Involves PII
- Yes
- Privacy Impact Assessment
- Not reported
- Authorization to Operate
- Yes
- Demographic features
- k) None of the above
- Training and evaluation data
- Completed 483 forms before redaction and versions of those forms after redaction by FDA staff
- Federal Data Catalog
- Not reported
Governance
0 of 8 minimum-practice questions answered. A blank answer means the agency reported nothing; it does not mean the practice is absent.
Potential impacts and how they were identified
Not reported