U.S. Food and Drug Administration Office of Regulatory Science
E886013
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.
All labels observed (1)
| Label | Occurrences |
|---|---|
| U.S. Food and Drug Administration Office of Regulatory Science canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T10790391 — 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 Regulatory Science Context triple: [White Oak, Maryland, isNearFederalFacility, U.S. Food and Drug Administration Office of Regulatory Science]
-
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.
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B.
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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C.
Center for Biologics Evaluation and Research
The Center for Biologics Evaluation and Research is the U.S. regulatory body responsible for overseeing the safety, efficacy, and quality of biological products such as vaccines, blood products, and gene therapies.
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D.
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.
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E.
Office of Pharmaceutical Quality
The Office of Pharmaceutical Quality is a U.S. Food and Drug Administration office responsible for ensuring the quality, safety, and consistency of human drugs throughout their lifecycle.
- 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 Regulatory Science Target entity description: 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.
-
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.
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.
-
C.
Center for Biologics Evaluation and Research
The Center for Biologics Evaluation and Research is the U.S. regulatory body responsible for overseeing the safety, efficacy, and quality of biological products such as vaccines, blood products, and gene therapies.
-
D.
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.
-
E.
Office of Pharmaceutical Quality
The Office of Pharmaceutical Quality is a U.S. Food and Drug Administration office responsible for ensuring the quality, safety, and consistency of human drugs throughout their lifecycle.
- F. None of above. chosen
Statements (49)
| Predicate | Object |
|---|---|
| instanceOf |
government office
ⓘ
scientific research organization ⓘ |
| activity |
conduct laboratory analysis
ⓘ
conduct risk-based research on emerging hazards ⓘ conduct scientific research ⓘ develop analytical methods ⓘ develop regulatory science tools ⓘ provide scientific support for enforcement actions ⓘ provide scientific support for inspections ⓘ validate test methods for regulatory use ⓘ |
| affiliation | U.S. Department of Health and Human Services NERFINISHED ⓘ |
| collaboratesWith |
academic research institutions
ⓘ
international regulatory partners ⓘ other FDA centers ⓘ other federal science agencies ⓘ state public health laboratories ⓘ |
| country |
United States of America
ⓘ
surface form:
United States
|
| employer |
chemist
ⓘ
federal scientist ⓘ laboratory analyst ⓘ microbiologist ⓘ quality systems specialist ⓘ regulatory scientist ⓘ toxicologist ⓘ |
| field |
analytical chemistry
ⓘ
biotechnology ⓘ food safety ⓘ laboratory quality systems ⓘ medical product safety ⓘ microbiology ⓘ pharmaceutical science ⓘ public health ⓘ regulatory science ⓘ toxicology ⓘ |
| focusesOn |
emerging technologies in product testing
ⓘ
evidence-based regulatory decisions ⓘ standardization of laboratory practices ⓘ |
| jurisdiction | federal jurisdiction of the United States ⓘ |
| location |
United States of America
ⓘ
surface form:
United States
|
| parentOrganization | Office of Regulatory Affairs NERFINISHED ⓘ |
| partOf | U.S. Food and Drug Administration NERFINISHED ⓘ |
| purpose |
ensure effectiveness of FDA-regulated products
ⓘ
ensure quality of FDA-regulated products ⓘ ensure safety of FDA-regulated products ⓘ support FDA regulatory decision-making ⓘ |
| regulates |
biologics testing methods
ⓘ
drug quality testing methods ⓘ food safety testing methods ⓘ medical device testing methods ⓘ |
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 Regulatory Science Description of subject: 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.
Referenced by (1)
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 Regulatory Science
ⓘ