EMA
E23502
EMA is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines.
All labels observed (1)
| Label | Occurrences |
|---|---|
| EMA canonical | 8 |
How this entity was disambiguated
This entity first appeared as the object of triple T184461 — 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: EMA Context triple: [European Medicines Agency, abbreviation, EMA]
-
A.
EMD
EMD is the commonly used abbreviation for the Engineering Management Division, a professional group focused on the practice and advancement of engineering management.
-
B.
EGA
EGA is the common abbreviation for the Eagle, Globe, and Anchor emblem that symbolizes the United States Marine Corps.
-
C.
EC
EC is the two-letter ISO 3166-1 alpha-2 country code assigned to Ecuador.
-
D.
ACE
ACE (Altamont Corridor Express) is a commuter rail service in California’s San Joaquin Valley and East Bay that provides weekday trains between Stockton and San Jose.
-
E.
E
The E is a New York City Subway line that runs between Queens and Manhattan, providing a key rapid transit connection used by AirTrain JFK passengers traveling to and from the city.
- 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: EMA Target entity description: EMA is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines.
-
A.
EMD
EMD is the commonly used abbreviation for the Engineering Management Division, a professional group focused on the practice and advancement of engineering management.
-
B.
EGA
EGA is the common abbreviation for the Eagle, Globe, and Anchor emblem that symbolizes the United States Marine Corps.
-
C.
EC
EC is the two-letter ISO 3166-1 alpha-2 country code assigned to Ecuador.
-
D.
ACE
ACE (Altamont Corridor Express) is a commuter rail service in California’s San Joaquin Valley and East Bay that provides weekday trains between Stockton and San Jose.
-
E.
E
The E is a New York City Subway line that runs between Queens and Manhattan, providing a key rapid transit connection used by AirTrain JFK passengers traveling to and from the city.
- F. None of above. chosen
Statements (47)
| Predicate | Object |
|---|---|
| instanceOf |
European Union agency
ⓘ
medicines regulatory authority ⓘ |
| abbreviation | EMA ⓘ |
| alsoKnownAs |
European Medicines Evaluation Agency
ⓘ
linked to:
European Medicines Agency
|
| cooperatesWith |
European Centre for Disease Prevention and Control
ⓘ
European Commission ⓘ World Health Organization ⓘ national medicines regulatory authorities in EU Member States ⓘ |
| country | European Union ⓘ |
| dateFounded | 1995 ⓘ |
| employs |
regulatory professionals
ⓘ
scientific experts ⓘ |
| foundedBy | European Union ⓘ |
| hasCommittee |
Committee for Advanced Therapies
ⓘ
Committee for Medicinal Products for Human Use ⓘ Committee for Medicinal Products for Veterinary Use ⓘ Committee for Orphan Medicinal Products ⓘ Pediatric Committee ⓘ
linked to:
Paediatric Committee
Pharmacovigilance Risk Assessment Committee ⓘ |
| hasMainRole |
safety monitoring of medicines
ⓘ
scientific evaluation of medicines ⓘ supervision of medicines ⓘ |
| hasScope | European Economic Area ⓘ |
| headquartersCountry | Netherlands ⓘ |
| headquartersLocation | Amsterdam ⓘ |
| jurisdiction | European Union ⓘ |
| language | English ⓘ |
| legalBasis | European Union pharmaceutical legislation ⓘ |
| locatedInTimeZone | Central European Time ⓘ |
| overseesProcess | centralised marketing authorisation of medicines ⓘ |
| predecessor |
European Agency for the Evaluation of Medicinal Products
ⓘ
linked to:
European Medicines Agency
|
| regulates |
medicinal products for human use
ⓘ
veterinary medicinal products ⓘ |
| responsibleFor |
coordination of safety monitoring of medicines
ⓘ
evaluation of applications for marketing authorisation ⓘ monitoring the safety of authorised medicines ⓘ pharmacovigilance in the European Union ⓘ providing scientific advice on medicine development ⓘ publishing safety communications on medicines ⓘ |
| sector |
pharmaceutical regulation
ⓘ
public health ⓘ |
| shortName | EMA ⓘ |
| subjectArea |
clinical trials assessment
ⓘ
drug safety ⓘ medicines regulation ⓘ |
| supervisedBy | European Commission ⓘ |
| website | https://www.ema.europa.eu ⓘ |
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: EMA Description of subject: EMA is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines.
Referenced by (8)
Full triples — surface form annotated when it differs from this entity's canonical label.