House Appropriations Committee Mandates FDA Medical Device Review and Food Inspection Reporting for Fiscal Year 2027

The House Appropriations Committee recently released its report for the Fiscal Year 2027 Agriculture, Rural Development, Food and Drug Administration, and Related Agencies appropriations bill, outlining specific funding levels and policy directives for the FDA. The report mandates that the agency prioritize the modernization of its regulatory processes, specifically regarding the review of medical devices and food safety protocols, while also imposing new reporting requirements on administrative expenditures. These directives signal a shift in congressional oversight, as lawmakers demand greater transparency and efficiency in how the agency allocates its resources across its various centers.

The committee’s report details several key areas of focus, including a directive for the FDA to reduce the backlog of pending premarket submissions for medical devices by the end of the fiscal year. Furthermore, the document instructs the agency to provide a comprehensive analysis of its current food inspection staffing levels, citing concerns over the frequency of facility audits. In addition to these operational mandates, the report restricts the use of appropriated funds for certain internal reorganizations unless the agency receives prior approval from the committee. These requirements aim to ensure that the FDA aligns its spending with the specific legislative priorities established by Congress for the upcoming fiscal cycle.

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Date: June 24, 2026

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GOAI