Triple
T22503948
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Medidata Solutions |
E556341
|
entity |
| Predicate | product |
P490
|
FINISHED |
| Object |
Medidata Rave eCOA
Medidata Rave eCOA is a clinical trial software solution that enables the electronic collection and management of patient-reported outcomes and clinical assessments on mobile devices.
|
E556341
|
NE FINISHED |
How this triple was built (4 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 eCOA | Statement: [Medidata Solutions, product, Medidata Rave eCOA]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Medidata Rave eCOA Context triple: [Medidata Solutions, product, Medidata Rave eCOA]
-
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.
eCTD
eCTD (electronic Common Technical Document) is a standardized, electronic format for submitting regulatory information on pharmaceuticals to health authorities worldwide.
-
E.
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.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg
Description generation
gpt-5.1
Instruction
Generate a one-sentence description of the target entity. You are given a context triple in the form (subject, predicate, object), where the object is the target entity. # Instructions Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. Avoid repeating the information from the triple, unless really essential. # Response Format Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: Medidata Rave eCOA Triple: [Medidata Solutions, product, Medidata Rave eCOA]
Generated description
Medidata Rave eCOA is a clinical trial software solution that enables the electronic collection and management of patient-reported outcomes and clinical assessments on mobile devices.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Medidata Rave eCOA Target entity description: Medidata Rave eCOA is a clinical trial software solution that enables the electronic collection and management of patient-reported outcomes and clinical assessments on mobile devices.
-
A.
Medidata Solutions
chosen
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.
eCTD
eCTD (electronic Common Technical Document) is a standardized, electronic format for submitting regulatory information on pharmaceuticals to health authorities worldwide.
-
E.
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.
- F. None of above.
Provenance (5 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. |
| NED1 | Entity disambiguation (via context triple) | batch_6a0b17e860888190b5c74df43a9890e9 |
completed | May 18, 2026, 1:45 p.m. |
| NEDg | Description generation | batch_6a0b18ad4f608190a6947aeb790d8be7 |
completed | May 18, 2026, 1:48 p.m. |
| NED2 | Entity disambiguation (via description) | batch_6a0b1979fe088190a06edb086d6b2b46 |
completed | May 18, 2026, 1:51 p.m. |
Created at: April 16, 2026, 8:50 p.m.