Triple
T23516986
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Central Drugs Standard Control Organisation |
E574393
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | medical device regulatory agency |
C1181
|
CONCEPT FINISHED |
How this triple was built (1 step)
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.
CD
Concept disambiguation
gpt-5-mini-2025-08-07
Target class: medical device regulatory agency Context triple: [Central Drugs Standard Control Organisation, instanceOf, medical device regulatory agency]
-
A.
medical device regulation system
A medical device regulation system is a framework of processes, rules, and oversight mechanisms that govern the evaluation, approval, monitoring, and post-market surveillance of medical devices to ensure their safety, effectiveness, and compliance with regulatory standards.
-
B.
medical device
A medical device is any instrument, apparatus, machine, implant, or similar article intended for use in diagnosing, preventing, monitoring, treating, or alleviating disease or other medical conditions in humans or animals.
-
C.
center of the U.S. Food and Drug Administration
The center of the U.S. Food and Drug Administration is the primary organizational unit within the FDA responsible for regulating and overseeing a specific category of products, such as drugs, biologics, or medical devices, to ensure their safety and effectiveness.
-
D.
regulatory agency component
A regulatory agency component is a modular part of a regulatory body responsible for performing specific oversight, rulemaking, enforcement, or compliance functions within a defined domain.
-
E.
regulatory authority
chosen
A regulatory authority is an official body empowered by law to create, implement, and enforce rules and standards within a specific domain to protect public interests and ensure compliance.
- F. None of above.
Provenance (1 batch)
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_69e245bb3dcc8190ba9a2b35972b58d0 |
completed | April 17, 2026, 2:37 p.m. |
Created at: April 17, 2026, 6:08 p.m.