U.S. Food and Drug Administration Office of Operations
E887234
The U.S. Food and Drug Administration Office of Operations is the FDA component responsible for overseeing the agency’s administrative, financial, and operational support functions across its programs and facilities.
All labels observed (2)
| Label | Occurrences |
|---|---|
| FDA Office of Operations | 1 |
| U.S. Food and Drug Administration Office of Operations canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T10790393 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: U.S. Food and Drug Administration Office of Operations Context triple: [White Oak, Maryland, isNearFederalFacility, U.S. Food and Drug Administration Office of Operations]
-
A.
U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy
The U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy is an FDA division responsible for overseeing and coordinating the agency’s worldwide regulatory, inspection, and compliance activities.
-
B.
U.S. Food and Drug Administration Office of the Commissioner
The U.S. Food and Drug Administration Office of the Commissioner is the central executive office that provides overall leadership, policy direction, and oversight for all FDA regulatory and public health activities.
-
C.
U.S. Food and Drug Administration Office of Regulatory Science
The U.S. Food and Drug Administration Office of Regulatory Science is an FDA division that conducts scientific research and analysis to support regulatory decisions on the safety, effectiveness, and quality of food, drugs, and other products under the agency’s oversight.
-
D.
Office of Regulatory Affairs
The Office of Regulatory Affairs is the U.S. FDA’s primary field organization responsible for inspecting regulated products and manufacturers, enforcing compliance, and overseeing import operations to protect public health.
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E.
U.S. Food and Drug Administration Office of Medical Products and Tobacco
The U.S. Food and Drug Administration Office of Medical Products and Tobacco is an FDA division responsible for overseeing the safety, effectiveness, and regulation of medical products and tobacco in the United States.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: U.S. Food and Drug Administration Office of Operations Target entity description: The U.S. Food and Drug Administration Office of Operations is the FDA component responsible for overseeing the agency’s administrative, financial, and operational support functions across its programs and facilities.
-
A.
U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy
The U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy is an FDA division responsible for overseeing and coordinating the agency’s worldwide regulatory, inspection, and compliance activities.
-
B.
U.S. Food and Drug Administration Office of the Commissioner
The U.S. Food and Drug Administration Office of the Commissioner is the central executive office that provides overall leadership, policy direction, and oversight for all FDA regulatory and public health activities.
-
C.
U.S. Food and Drug Administration Office of Regulatory Science
The U.S. Food and Drug Administration Office of Regulatory Science is an FDA division that conducts scientific research and analysis to support regulatory decisions on the safety, effectiveness, and quality of food, drugs, and other products under the agency’s oversight.
-
D.
Office of Regulatory Affairs
The Office of Regulatory Affairs is the U.S. FDA’s primary field organization responsible for inspecting regulated products and manufacturers, enforcing compliance, and overseeing import operations to protect public health.
-
E.
U.S. Food and Drug Administration Office of Medical Products and Tobacco
The U.S. Food and Drug Administration Office of Medical Products and Tobacco is an FDA division responsible for overseeing the safety, effectiveness, and regulation of medical products and tobacco in the United States.
- F. None of above. chosen
Statements (28)
| Predicate | Object |
|---|---|
| instanceOf |
FDA office
ⓘ
government administrative unit ⓘ |
| abbreviation | FDA Office of Operations ⓘ |
| country |
United States
ⓘ
linked to:
United States of America
|
| employer | federal civil service employees ⓘ |
| function | internal management and operations support ⓘ |
| goal | ensure effective and efficient FDA operations ⓘ |
| governingLaw | U.S. federal law ⓘ |
| jurisdiction | federal ⓘ |
| languageOfWork | English ⓘ |
| locatedIn | United States Department of Health and Human Services organizational structure ⓘ |
| organizationType | headquarters support office ⓘ |
| oversees |
administrative support functions of FDA
ⓘ
financial management support functions of FDA ⓘ operational support functions of FDA ⓘ |
| parentAgency |
U.S. Food and Drug Administration
ⓘ
linked to:
Food and Drug Administration
|
| partOf |
U.S. Food and Drug Administration
ⓘ
linked to:
Food and Drug Administration
|
| regulatoryAuthority | does not directly regulate products ⓘ |
| responsibleFor |
agency-wide administrative policy implementation
ⓘ
agency-wide financial policy implementation ⓘ agency-wide operational policy implementation ⓘ |
| scopeOfResponsibility |
FDA facilities
ⓘ
FDA programs ⓘ |
| sector | public health regulation support ⓘ |
| supports |
FDA field operations infrastructure
ⓘ
FDA headquarters operations infrastructure ⓘ FDA mission ⓘ |
| worksWith | other FDA centers and offices ⓘ |
How these facts were elicited
The pipeline generated the facts above by prompting gpt-5.1 with this entity's name + description and the instruction below.
Instruction
You are a knowledge base construction expert. Given a subject entity and a description of it, return factual statements that you know for the subject as a JSON list of dictionaries(triples), where keys must be "subject", "predicate" and "object". The number of facts may be very high, between 25 to 50 or more, for very popular subjects. For less popular subjects, the number of facts can be very low, like 5 or 10. # Requirements - If you don't know the subject at all, return an empty list. - If the subject is not a named entity, return an empty list. - Include at least one triple where predicate is "instanceOf". - Do not get too wordy. - Separate several objects into multiple triples with one object.
Input
Subject: U.S. Food and Drug Administration Office of Operations Description of subject: The U.S. Food and Drug Administration Office of Operations is the FDA component responsible for overseeing the agency’s administrative, financial, and operational support functions across its programs and facilities.
Referenced by (2)
Full triples — surface form annotated when it differs from this entity's canonical label.
White Oak, Maryland
→
isNearFederalFacility
→
U.S. Food and Drug Administration Office of Operations
ⓘ
linked to: U.S. Food and Drug Administration Office of Operations