Commission Regulation (EC) No 507/2006
E1474270
UNEXPLORED
Commission Regulation (EC) No 507/2006 is an EU legal act that sets the rules and procedures for granting conditional marketing authorizations for medicinal products for human use.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Commission Regulation (EC) No 507/2006 canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T21228251 — 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: Commission Regulation (EC) No 507/2006 Context triple: [Conditional Marketing Authorization by European Medicines Agency, regulatedBy, Commission Regulation (EC) No 507/2006]
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A.
Council Regulation (EC) No 510/2006
Council Regulation (EC) No 510/2006 was an EU law establishing the system for protecting geographical indications and designations of origin for agricultural products and foodstuffs before being replaced by Regulation (EU) No 1151/2012.
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B.
Council Regulation (EC) No 768/2005
Council Regulation (EC) No 768/2005 is a European Union legal act that established the framework for creating the European Fisheries Control Agency and harmonizing fisheries control and inspection across member states.
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C.
Regulation (EC) No 1901/2006
Regulation (EC) No 1901/2006 is the European Union’s Paediatric Regulation, establishing rules to ensure that medicines for children are researched, developed, and authorized to the same high standards as those for adults.
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D.
Council Regulation (EC) No 6/2002
Council Regulation (EC) No 6/2002 is a key European Union legislative act that establishes the legal framework for Community designs, including their registration, protection, and enforcement across the EU.
-
E.
Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
- 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: Commission Regulation (EC) No 507/2006 Target entity description: Commission Regulation (EC) No 507/2006 is an EU legal act that sets the rules and procedures for granting conditional marketing authorizations for medicinal products for human use.
-
A.
Council Regulation (EC) No 510/2006
Council Regulation (EC) No 510/2006 was an EU law establishing the system for protecting geographical indications and designations of origin for agricultural products and foodstuffs before being replaced by Regulation (EU) No 1151/2012.
-
B.
Council Regulation (EC) No 768/2005
Council Regulation (EC) No 768/2005 is a European Union legal act that established the framework for creating the European Fisheries Control Agency and harmonizing fisheries control and inspection across member states.
-
C.
Regulation (EC) No 1901/2006
Regulation (EC) No 1901/2006 is the European Union’s Paediatric Regulation, establishing rules to ensure that medicines for children are researched, developed, and authorized to the same high standards as those for adults.
-
D.
Council Regulation (EC) No 6/2002
Council Regulation (EC) No 6/2002 is a key European Union legislative act that establishes the legal framework for Community designs, including their registration, protection, and enforcement across the EU.
-
E.
Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.
Conditional Marketing Authorization by European Medicines Agency
→
regulatedBy
→
Commission Regulation (EC) No 507/2006
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