Directive 2004/28/EC
E1537150
UNEXPLORED
Directive 2004/28/EC is a European Union legislative act that revised and updated the legal framework for the authorization, supervision, and pharmacovigilance of veterinary medicinal products.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 2004/28/EC canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T22452710 — 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: Directive 2004/28/EC Context triple: [Directive 2001/82/EC, amendedBy, Directive 2004/28/EC]
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A.
Directive 2004/27/EC
Directive 2004/27/EC is a European Union legislative act that revised and updated the Community code relating to medicinal products for human use, strengthening rules on authorization, supervision, and pharmacovigilance.
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B.
Directive 2004/24/EC
Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
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C.
Directive 2004/23/EC
Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
-
D.
Directive 2002/58/EC
Directive 2002/58/EC is a European Union directive that sets out rules on privacy and data protection in the electronic communications sector, complementing the broader EU data protection framework.
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E.
Directive 2007/47/EC
Directive 2007/47/EC is a European Union legislative act that updated and strengthened the regulatory framework for medical devices, active implantable medical devices, and in vitro diagnostic medical devices to improve safety and harmonization across member 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: Directive 2004/28/EC Target entity description: Directive 2004/28/EC is a European Union legislative act that revised and updated the legal framework for the authorization, supervision, and pharmacovigilance of veterinary medicinal products.
-
A.
Directive 2004/27/EC
Directive 2004/27/EC is a European Union legislative act that revised and updated the Community code relating to medicinal products for human use, strengthening rules on authorization, supervision, and pharmacovigilance.
-
B.
Directive 2004/24/EC
Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
-
C.
Directive 2004/23/EC
Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
-
D.
Directive 2002/58/EC
Directive 2002/58/EC is a European Union directive that sets out rules on privacy and data protection in the electronic communications sector, complementing the broader EU data protection framework.
-
E.
Directive 2007/47/EC
Directive 2007/47/EC is a European Union legislative act that updated and strengthened the regulatory framework for medical devices, active implantable medical devices, and in vitro diagnostic medical devices to improve safety and harmonization across member states.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.