Triple

T22457762
Position Surface form Disambiguated ID Type / Status
Subject ICH E2A E555157 entity
Predicate fullTitle P1116 FINISHED
Object Clinical Safety Data Management: Definitions and Standards for Expedited Reporting — NE NERFINISHED

How this triple was built (2 steps)

Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.

NER Named-entity recognition gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: Clinical Safety Data Management: Definitions and Standards for Expedited Reporting | Statement: [ICH E2A, fullTitle, Clinical Safety Data Management: Definitions and Standards for Expedited Reporting]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Clinical Safety Data Management: Definitions and Standards for Expedited Reporting
Context triple: [ICH E2A, fullTitle, Clinical Safety Data Management: Definitions and Standards for Expedited Reporting]
  • A. ICH E2A Clinical Safety Data Management chosen
    ICH E2A Clinical Safety Data Management is an international guideline that standardizes the collection, reporting, and evaluation of clinical safety data in drug development to support consistent pharmacovigilance and regulatory decision-making.
  • B. Patient Safety and Adverse Events Composite
    The Patient Safety and Adverse Events Composite is a standardized quality measure that summarizes multiple hospital-acquired complications and safety-related adverse events into a single score to assess and compare inpatient safety performance.
  • C. Fast Healthcare Interoperability Resources
    Fast Healthcare Interoperability Resources (FHIR) is a modern, web-based standard for exchanging electronic healthcare information between systems in a consistent and interoperable way.
  • D. Pharmacovigilance Risk Assessment Committee within the European Medicines Agency
    The Pharmacovigilance Risk Assessment Committee within the European Medicines Agency is an expert body responsible for evaluating and monitoring the safety of medicines across the European Union and providing recommendations on managing and communicating medicine-related risks.
  • E. Central Data Repository for regulatory reports
    The Central Data Repository for regulatory reports is a centralized system used by U.S. financial regulators to collect, store, and manage standardized regulatory reporting data from financial institutions.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

Provenance (2 batches)

The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.

Step Stage Batch ID Status When
creating Elicitation batch_69e11e51fdec8190adfdf9f8a6362221 completed April 16, 2026, 5:37 p.m.
NER Named-entity recognition batch_69f15b7d00208190955a70e2c22d25a4 completed April 29, 2026, 1:14 a.m.
Created at: April 16, 2026, 8:48 p.m.