*GUDID Migration to the FURLS Platform - Agency IT Modernization

This proposal to support the migration of the Global Unique Device Identification Database (GUDID) into the FDA Unified Registration and Listing System (FURLS) as an integrated module, consolidating the three complementary domains of medical device regulation - establishment registration, device listing, and unique device identification - into a single, cohesive platform. GUDID currently operates as a standalone application with limited cross-system integrations and validations, contributing to data quality challenges and an artificial regulatory separation that impedes holistic oversight of the medical device ecosystem. Migrating GUDID into FURLS will eliminate platform redundancy, strengthen data integrity through cross-system validation, and deliver measurable gains in regulatory efficiency and analytical capability in support of the CDRH's review tools and performance analytics functions. This effort directly advances FDA's agency IT consolidation strategy and aligns with CDRH priorities in Regulatory Efficiency & Modernization, as well as FDA's broader commitment to Innovation and Global Leadership. Contractor services will provide the technical expertise necessary to design, develop, test, and deploy the GUDID-FURLS integration within the fiscal year, ensuring continuity of operations and minimal disruption to regulated industry.

Estimated value

>= $1.5M and < $3M

Est. solicitation date

Jul 1, 2026

Anticipated award

Jan 1, 2027