Center for Biologics Evaluation and Research
E86214
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.
All labels observed (6)
How this entity was disambiguated
This entity first appeared as the object of triple T686645 — 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.
Target entity: Center for Biologics Evaluation and Research Context triple: [Food and Drug Administration, hasDivision, Center for Biologics Evaluation and Research]
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A.
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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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.
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C.
Center for Scientific Review
The Center for Scientific Review is the National Institutes of Health component responsible for overseeing the peer review of most grant applications to ensure scientific merit and integrity in funding decisions.
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D.
National Institutes of Health
The National Institutes of Health is the United States’ primary federal biomedical research agency, supporting and conducting medical research to improve public health.
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E.
National Center for Advancing Translational Sciences
The National Center for Advancing Translational Sciences is a U.S. biomedical research center focused on accelerating the development and delivery of new diagnostics, treatments, and cures by improving the translational science process.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Target entity: Center for Biologics Evaluation and Research Target entity description: 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.
-
A.
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.
-
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 Scientific Review
The Center for Scientific Review is the National Institutes of Health component responsible for overseeing the peer review of most grant applications to ensure scientific merit and integrity in funding decisions.
-
D.
National Institutes of Health
The National Institutes of Health is the United States’ primary federal biomedical research agency, supporting and conducting medical research to improve public health.
-
E.
National Center for Advancing Translational Sciences
The National Center for Advancing Translational Sciences is a U.S. biomedical research center focused on accelerating the development and delivery of new diagnostics, treatments, and cures by improving the translational science process.
- F. None of above. chosen
Statements (47)
| Predicate | Object |
|---|---|
| instanceOf |
U.S. Food and Drug Administration center
ⓘ
regulatory agency ⓘ |
| collaboratesWith |
Centers for Disease Control and Prevention
ⓘ
National Institutes of Health ⓘ World Health Organization ⓘ |
| conducts | regulatory science research on biologics ⓘ |
| country |
United States of America
ⓘ
surface form:
United States
|
| foundedBy |
United States government
ⓘ
surface form:
U.S. federal government
|
| hasDivision |
Office of Biostatistics
ⓘ
surface form:
Office of Biostatistics and Pharmacovigilance
Center for Biologics Evaluation and Research self-linksurface differs ⓘ
surface form:
Office of Blood Research and Review
Office of Compliance and Biologics Quality ⓘ Office of Tissues and Advanced Therapies ⓘ Center for Biologics Evaluation and Research self-linksurface differs ⓘ
surface form:
Office of Vaccines Research and Review
|
| headquartersFacility |
White Oak Federal Research Center
ⓘ
surface form:
FDA White Oak Campus
|
| headquartersLocation | Silver Spring, Maryland ⓘ |
| issues |
biologics regulations and policies
ⓘ
guidance documents for industry on biologics ⓘ |
| jurisdiction |
United States of America
ⓘ
surface form:
United States
|
| language | English ⓘ |
| mission |
to ensure the safety, purity, potency, and effectiveness of biological products
ⓘ
to protect and advance public health through regulation of biologics ⓘ |
| monitors |
adverse events related to blood products
ⓘ
adverse events related to gene therapies ⓘ adverse events related to vaccines ⓘ |
| oversees |
biologics license applications
ⓘ
blood establishment licensing ⓘ good manufacturing practice compliance for biologics ⓘ investigational new drug applications for biologics ⓘ post-market surveillance of biologics ⓘ pre-market review of biologics ⓘ vaccine safety monitoring ⓘ |
| parentOrganization |
United States Department of Health and Human Services
ⓘ
surface form:
U.S. Department of Health and Human Services
Food and Drug Administration ⓘ
surface form:
U.S. Food and Drug Administration
|
| partOf |
Public Health Service
ⓘ
surface form:
U.S. Public Health Service
|
| regulates |
allergenics
ⓘ
biological products ⓘ blood products ⓘ cellular therapies ⓘ certain diagnostic tests for blood safety ⓘ certain medical devices related to blood and tissues ⓘ gene therapies ⓘ plasma-derived products ⓘ tissue-based products ⓘ vaccines ⓘ xenotransplantation products ⓘ |
| shortName |
Center for Biologics Evaluation and Research
self-linksurface differs
ⓘ
surface form:
CBER
|
| website | https://www.fda.gov/about-fda/center-biologics-evaluation-and-research-cber ⓘ |
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.
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.
Subject: Center for Biologics Evaluation and Research Description of subject: 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.
Referenced by (12)
Full triples — surface form annotated when it differs from this entity's canonical label.