Good Laboratory Practice
E1342265
UNEXPLORED
Good Laboratory Practice (GLP) is a quality system of management controls for research laboratories that ensures the consistency, reliability, and integrity of non-clinical safety studies, particularly for regulatory submissions.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Good Laboratory Practice canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T18750408 — 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: Good Laboratory Practice Context triple: [Good Manufacturing Practices, isRelatedTo, Good Laboratory Practice]
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A.
Good Manufacturing Practices
Good Manufacturing Practices are a set of regulatory and industry standards that ensure products are consistently produced and controlled to quality and safety requirements, particularly in sectors like food, pharmaceuticals, and cosmetics.
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B.
GMP
GMP is the IATA airport code for Gimpo International Airport, a major airport serving the Seoul metropolitan area in South Korea.
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C.
ICH Q11 Development and Manufacture of Drug Substances
ICH Q11 Development and Manufacture of Drug Substances is an ICH guideline that provides principles and expectations for the development and manufacturing of chemical and biotechnological drug substances within a quality-by-design framework.
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D.
ICH E6 Good Clinical Practice
ICH E6 Good Clinical Practice is an international ethical and scientific quality standard that governs the design, conduct, recording, and reporting of clinical trials involving human subjects.
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E.
ICH Q10 Pharmaceutical Quality System
ICH Q10 Pharmaceutical Quality System is an international guideline that establishes a comprehensive, lifecycle-based framework for pharmaceutical quality management to ensure consistent product quality and regulatory compliance.
- 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: Good Laboratory Practice Target entity description: Good Laboratory Practice (GLP) is a quality system of management controls for research laboratories that ensures the consistency, reliability, and integrity of non-clinical safety studies, particularly for regulatory submissions.
-
A.
Good Manufacturing Practices
Good Manufacturing Practices are a set of regulatory and industry standards that ensure products are consistently produced and controlled to quality and safety requirements, particularly in sectors like food, pharmaceuticals, and cosmetics.
-
B.
GMP
GMP is the IATA airport code for Gimpo International Airport, a major airport serving the Seoul metropolitan area in South Korea.
-
C.
ICH Q11 Development and Manufacture of Drug Substances
ICH Q11 Development and Manufacture of Drug Substances is an ICH guideline that provides principles and expectations for the development and manufacturing of chemical and biotechnological drug substances within a quality-by-design framework.
-
D.
ICH E6 Good Clinical Practice
ICH E6 Good Clinical Practice is an international ethical and scientific quality standard that governs the design, conduct, recording, and reporting of clinical trials involving human subjects.
-
E.
ICH Q10 Pharmaceutical Quality System
ICH Q10 Pharmaceutical Quality System is an international guideline that establishes a comprehensive, lifecycle-based framework for pharmaceutical quality management to ensure consistent product quality and regulatory compliance.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.