Directive 2006/17/EC
E619864
Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 2006/17/EC canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T6769628 — 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: Directive 2006/17/EC Context triple: [EU Tissues and Cells Directives, includes, Directive 2006/17/EC]
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A.
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.
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B.
Directive 2009/147/EC
Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
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C.
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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D.
Directive 2006/86/EC
Directive 2006/86/EC is a European Union legal act that sets detailed technical requirements for the traceability, notification of serious adverse reactions and events, and quality and safety standards for human tissues and cells used in medical treatments.
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E.
Directive 2001/82/EC
Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Target entity: Directive 2006/17/EC Target entity description: Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
-
A.
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.
-
B.
Directive 2009/147/EC
Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
-
C.
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.
-
D.
Directive 2006/86/EC
Directive 2006/86/EC is a European Union legal act that sets detailed technical requirements for the traceability, notification of serious adverse reactions and events, and quality and safety standards for human tissues and cells used in medical treatments.
-
E.
Directive 2001/82/EC
Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
- F. None of above. chosen
Statements (42)
| Predicate | Object |
|---|---|
| instanceOf | European Union directive ⓘ |
| adoptedBy | European Commission NERFINISHED ⓘ |
| aimsTo |
ensure high level of human health protection
ⓘ
ensure quality and safety of human tissues and cells ⓘ prevent transmission of diseases through tissues and cells ⓘ |
| appliesTo |
Member States of the European Union
NERFINISHED
ⓘ
healthcare facilities using human tissues and cells ⓘ tissue establishments ⓘ |
| basedOn | scientific and technical progress in tissues and cells ⓘ |
| belongsTo | EU acquis on substances of human origin ⓘ |
| complements | Directive 2004/23/EC NERFINISHED ⓘ |
| concerns |
quality control in tissue and cell procurement
ⓘ
safety of recipients of human tissues and cells ⓘ |
| form | binding legislative act ⓘ |
| fullName | Commission Directive 2006/17/EC NERFINISHED ⓘ |
| instrumentFor | implementation of Directive 2004/23/EC technical requirements ⓘ |
| jurisdiction | European Union ⓘ |
| language | multilingual EU legal act ⓘ |
| legalBasis | Directive 2004/23/EC NERFINISHED ⓘ |
| legalNature | must be transposed into national law by Member States ⓘ |
| objective | harmonise minimum standards across EU Member States ⓘ |
| policyArea |
public health
ⓘ
quality and safety of human substances of human origin ⓘ tissues and cells safety ⓘ |
| regulates |
documentation and traceability requirements for tissues and cells
ⓘ
donor evaluation procedures ⓘ donor selection criteria ⓘ laboratory testing of donors ⓘ procurement procedures for tissues and cells ⓘ |
| requires |
biological testing of donors prior to use of tissues and cells
ⓘ
donor medical history assessment ⓘ informed consent procedures for donation of tissues and cells ⓘ record-keeping for tissues and cells from donation to human application ⓘ technical requirements for donation of human tissues and cells ⓘ technical requirements for procurement of human tissues and cells ⓘ technical requirements for testing of human tissues and cells ⓘ testing for communicable diseases in tissue and cell donors ⓘ |
| scope | human tissues and cells intended for human application ⓘ |
| subjectMatter |
donation of human tissues and cells
ⓘ
procurement of human tissues and cells ⓘ testing of human tissues and cells ⓘ |
| typeOfMeasure | technical implementing directive ⓘ |
How these facts were elicited
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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: Directive 2006/17/EC Description of subject: Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.