Triple

T22503946
Position Surface form Disambiguated ID Type / Status
Subject Medidata Solutions E556341 entity
Predicate product P490 FINISHED
Object Medidata Rave RTSM — NE NERFINISHED

How this triple was built (3 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: Medidata Rave RTSM | Statement: [Medidata Solutions, product, Medidata Rave RTSM]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Medidata Rave RTSM
Context triple: [Medidata Solutions, product, Medidata Rave RTSM]
  • A. Medidata Solutions
    Medidata Solutions is a life sciences technology company best known for its cloud-based clinical trial and research platforms used by pharmaceutical, biotech, and medical device organizations.
  • B. ICH E2A Clinical Safety Data Management
    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.
  • C. Clinical Trials Information System
    The Clinical Trials Information System is the EU’s centralized online portal and database for the submission, assessment, authorization, and public transparency of clinical trials conducted in the European Union.
  • D. Regenstrief Medical Record System
    The Regenstrief Medical Record System is an early, pioneering electronic medical record platform that helped shape modern health informatics and clinical data management practices.
  • E. Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs
    Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs (ICH E2C) is an international guideline that standardizes the format, content, and timing of periodic safety reports submitted by marketing authorization holders to monitor and communicate the ongoing safety profile of approved medicines.
  • 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: Medidata Rave RTSM
Target entity description: Medidata Rave RTSM is a clinical trial randomization and trial supply management solution integrated into the Medidata Rave platform to streamline patient allocation and study drug logistics.
  • A. Medidata Solutions
    Medidata Solutions is a life sciences technology company best known for its cloud-based clinical trial and research platforms used by pharmaceutical, biotech, and medical device organizations.
  • B. ICH E2A Clinical Safety Data Management
    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.
  • C. Clinical Trials Information System
    The Clinical Trials Information System is the EU’s centralized online portal and database for the submission, assessment, authorization, and public transparency of clinical trials conducted in the European Union.
  • D. Regenstrief Medical Record System
    The Regenstrief Medical Record System is an early, pioneering electronic medical record platform that helped shape modern health informatics and clinical data management practices.
  • E. Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs
    Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs (ICH E2C) is an international guideline that standardizes the format, content, and timing of periodic safety reports submitted by marketing authorization holders to monitor and communicate the ongoing safety profile of approved medicines.
  • F. None of above. chosen

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_69e11e555edc81909ca803587dafd747 completed April 16, 2026, 5:37 p.m.
NER Named-entity recognition batch_69f15d5ac5808190a66f9111c350f4dc completed April 29, 2026, 1:22 a.m.
Created at: April 16, 2026, 8:50 p.m.