Federal Service for State Registration of Medicines
E686044
The Federal Service for State Registration of Medicines is a Russian government agency responsible for evaluating, approving, and overseeing the circulation of pharmaceutical drugs within the country.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Federal Service for State Registration of Medicines canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T7756493 — 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: Federal Service for State Registration of Medicines Context triple: [Federal services of Russia, includes, Federal Service for State Registration of Medicines]
-
A.
Committee for Proprietary Medicinal Products
The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
-
B.
Centre for Drug Safety
The Centre for Drug Safety is a specialized unit within the Norwegian Institute of Public Health that focuses on monitoring, researching, and improving the safe use of medicines.
-
C.
Russian Federal Service for Intellectual Property
The Russian Federal Service for Intellectual Property is Russia’s national authority responsible for administering patents, trademarks, and other intellectual property rights.
-
D.
Pharmaceuticals and Medical Devices Agency Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) is Japan’s regulatory authority responsible for the review, approval, and safety monitoring of pharmaceuticals and medical devices.
-
E.
Center for Drug Evaluation and Research
The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
- 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: Federal Service for State Registration of Medicines Target entity description: The Federal Service for State Registration of Medicines is a Russian government agency responsible for evaluating, approving, and overseeing the circulation of pharmaceutical drugs within the country.
-
A.
Committee for Proprietary Medicinal Products
The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
-
B.
Centre for Drug Safety
The Centre for Drug Safety is a specialized unit within the Norwegian Institute of Public Health that focuses on monitoring, researching, and improving the safe use of medicines.
-
C.
Russian Federal Service for Intellectual Property
The Russian Federal Service for Intellectual Property is Russia’s national authority responsible for administering patents, trademarks, and other intellectual property rights.
-
D.
Pharmaceuticals and Medical Devices Agency Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) is Japan’s regulatory authority responsible for the review, approval, and safety monitoring of pharmaceuticals and medical devices.
-
E.
Center for Drug Evaluation and Research
The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
- F. None of above. chosen
Statements (32)
| Predicate | Object |
|---|---|
| instanceOf |
government agency
ⓘ
regulatory authority ⓘ |
| activity |
control of compliance with pharmaceutical legislation
ⓘ
granting marketing authorizations for medicines ⓘ maintaining state register of medicines ⓘ pharmacovigilance oversight ⓘ review of clinical trial data for medicines ⓘ |
| aim |
prevention of circulation of falsified medicines
ⓘ
prevention of circulation of substandard medicines ⓘ protection of public health ⓘ |
| country | Russia ⓘ |
| field |
drug regulation
ⓘ
public health regulation ⓘ |
| governedBy | Russian pharmaceutical legislation ⓘ |
| jurisdiction | Russian Federation NERFINISHED ⓘ |
| languageOfWork | Russian ⓘ |
| legalStatus | federal executive body ⓘ |
| regulates |
medicinal products
ⓘ
pharmaceutical drugs for human use ⓘ |
| responsibility |
approval of pharmaceutical drugs
ⓘ
ensuring efficacy of medicines ⓘ ensuring quality of medicines ⓘ ensuring safety of medicines ⓘ evaluation of pharmaceutical drugs ⓘ oversight of circulation of medicines ⓘ regulation of pharmaceutical market ⓘ state registration of medicines ⓘ |
| sector |
healthcare
ⓘ
pharmaceuticals ⓘ |
| supervises | circulation of medicines on Russian market ⓘ |
| typeOfRegulation |
post-market surveillance
ⓘ
pre-market authorization ⓘ |
How these facts were elicited
The pipeline generated the facts above by prompting gpt-5.1 with this entity's name + description and the instruction below.
Instruction
You are a knowledge base construction expert. Given a subject entity and a description of it, return factual statements that you know for the subject as a JSON list of dictionaries(triples), where keys must be "subject", "predicate" and "object". The number of facts may be very high, between 25 to 50 or more, for very popular subjects. For less popular subjects, the number of facts can be very low, like 5 or 10. # Requirements - If you don't know the subject at all, return an empty list. - If the subject is not a named entity, return an empty list. - Include at least one triple where predicate is "instanceOf". - Do not get too wordy. - Separate several objects into multiple triples with one object.
Input
Subject: Federal Service for State Registration of Medicines Description of subject: The Federal Service for State Registration of Medicines is a Russian government agency responsible for evaluating, approving, and overseeing the circulation of pharmaceutical drugs within the country.
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.
subject surface form:
Federal services of Russia