U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy
E886014
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.
All labels observed (2)
| Label | Occurrences |
|---|---|
| Office of Global Regulatory Operations and Policy | 1 |
| U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T10790395 — 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 Global Regulatory Operations and Policy Context triple: [White Oak, Maryland, isNearFederalFacility, U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy]
-
A.
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.
-
B.
Food and Drug Administration
The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
-
C.
Center for Drug Evaluation and Research
The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
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D.
FDA CFSAN
FDA CFSAN is the U.S. Food and Drug Administration’s center responsible for regulating the safety, labeling, and nutritional quality of foods, dietary supplements, and cosmetics.
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E.
Office of Orphan Products Development
The Office of Orphan Products Development is a U.S. Food and Drug Administration office that promotes the development of drugs and other medical products for rare diseases and conditions.
- 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 Global Regulatory Operations and Policy Target entity description: 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.
-
A.
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.
-
B.
Food and Drug Administration
The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
-
C.
Center for Drug Evaluation and Research
The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
-
D.
FDA CFSAN
FDA CFSAN is the U.S. Food and Drug Administration’s center responsible for regulating the safety, labeling, and nutritional quality of foods, dietary supplements, and cosmetics.
-
E.
Office of Orphan Products Development
The Office of Orphan Products Development is a U.S. Food and Drug Administration office that promotes the development of drugs and other medical products for rare diseases and conditions.
- F. None of above. chosen
Statements (33)
| Predicate | Object |
|---|---|
| instanceOf |
FDA office
ⓘ
government organization unit ⓘ |
| abbreviation |
OGROP
ⓘ
Office of Global Regulatory Operations and Policy ⓘ |
| coordinatesWith |
foreign regulatory authorities
ⓘ
international organizations ⓘ other FDA centers and offices ⓘ |
| country |
United States
ⓘ
linked to:
United States of America
|
| focusesOn |
compliance policy
ⓘ
inspection policy ⓘ regulatory policy ⓘ |
| hasRole |
coordinate worldwide compliance activities
ⓘ
coordinate worldwide inspection activities ⓘ oversee global regulatory activities ⓘ |
| jurisdiction |
FDA-regulated products
ⓘ
domestic regulatory operations ⓘ international regulatory operations ⓘ |
| locatedIn | United States federal government structure ⓘ |
| mission |
ensure consistent and effective global regulatory oversight
ⓘ
support FDA public health protection goals through compliance and enforcement ⓘ |
| parentOrganization | U.S. Department of Health and Human Services ⓘ |
| partOf |
U.S. Food and Drug Administration
ⓘ
linked to:
Food and Drug Administration
|
| regulates |
FDA compliance programs
ⓘ
FDA field operations ⓘ FDA inspection programs ⓘ |
| responsibleFor |
oversight of FDA field inspection activities
ⓘ
oversight of import and export regulatory activities ⓘ policy development for global regulatory operations ⓘ strategic planning for inspections and compliance ⓘ |
| scope |
global
ⓘ
worldwide regulatory operations ⓘ |
| sector |
food and drug regulation
ⓘ
public health regulation ⓘ |
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 Global Regulatory Operations and Policy Description of subject: 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.
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 Global Regulatory Operations and Policy
ⓘ
U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy
→
abbreviation
→
Office of Global Regulatory Operations and Policy
ⓘ
linked to: U.S. Food and Drug Administration Office of Global Regulatory Operations and Policy