Food and Drug Administration

Topics on this page: Summary of Activities that Continue | Summary of Contingency Staffing Plan

Summary of Activities that Continue

The Food and Drug Administration (FDA) activities funded through user fees will continue including the regulation and testing of human and animal drugs, biosimilars, medical devices, and tobacco products. User fee work specifically supports the approval of new medical products, the review of requests to conduct important clinical research, the issuance of guidance, and other necessary activities to help patients have access to new therapies and important generic and biosimilar treatment options.

All vital FDA activities related to imminent threats to human health or life will also continue. This includes detecting and responding to public health emergencies, continuing to address existing critical public health challenges, and managing recalls, including drug shortages, and outbreaks related to foodborne illness and infectious diseases.  Other vital activities that will continue are surveillance of adverse event reports for issues that could cause human harm, the review of import entries to determine potential risks to human health, determining conduct for cause and surveillance inspections of regulated facilities, and criminal enforcement work and certain civil investigations.

Summary of Contingency Staffing Plan

In the event of a lapse of appropriation, 13,133 (75%) of FDA staff will be retained including 9,017 (52%) who are exempt (their activities or position are already funded or otherwise exempted) and 4,116 (24%) who are excepted (their activities are deemed necessary by implication, or for the safety of human life or protection of property).

Exempt Staff:

A total of 9,017 (52%) FDA staff will be exempt. Exempt FDA staff include one HHS Officer appointed by the President and 9,016 staff who support activities that have funding available during a lapse in appropriations. These activities with funding available include user fee programs including the approval of new medical products, the ability to review requests to conduct important clinical research, issue guidance, and conduct other necessary activities to help patients have access to new therapies and important generic and biosimilar treatment options.

Excepted Staff:

A total of 4,116 (24%) FDA staff are considered excepted and can legally continue their activities in the absence of appropriations. These staff fall into three categories; 1) those whose work is necessary for the safety of human life, 2) those whose work is necessary for the protection of property, and 3) those whose work is "necessarily implied" from the authorized continuation of other activities or the need to phase down and suspend operations.

Excepted FDA staff will continue to perform vital tasks related to imminent threats to human health or life including detecting and responding to emergencies, managing recalls, pursuing criminal enforcement work and certain civil investigations, reviewing import entries to determine potential risks to human health, conducting for cause and surveillance inspections of regulated facilities, conducting surveillance of adverse events reports for issues that could cause human harm, and other critical public health issues as appropriate. These excepted staff will also be responsible for continuing efforts to address other serious public health challenges, including drug shortages, and outbreaks related to foodborne illness and infectious diseases.

Excepted staff will also continue activities ensuring the protection of government research property, animals, and inanimate property. Examples include the care and feeding of any animals associated with research activities and maintaining research property used for regulatory science research such as high performance computational equipment.

Additionally staff will also be considered exempt and continue to work if their duties are necessary to ensure the ongoing support and operations of funded activities, or if they are needed for the orderly phase down and suspension of non-funded activities. These FDA staff will continue to provide the necessary operational support to ensure the centers and offices can continue authorized and funded activities. For example, user fee work that supports the approval of new medical products (for both humans and animals), the ability to review requests to conduct important clinical research, issue guidance, and other necessary activities to help patients have access to new therapies and important generic and biosimilar treatment options.