Norwegian Medicines Agency

E119701

government agency medicines regulatory authority

The Norwegian Medicines Agency is Norway’s national regulatory authority responsible for the approval, monitoring, and safe use of medicines and related health products.

Try in SPARQL Jump to: Surface forms Statements Referenced by

All labels observed (2)

Label	Occurrences
Norwegian Medicines Agency canonical	2
Statens legemiddelverk	1

Statements (48)

Predicate	Object
instanceOf	government agency ⓘ medicines regulatory authority ⓘ
abbreviation	NoMA ⓘ
aimsTo	promote correct and effective use of medicines ⓘ protect patients from harmful medicines ⓘ
collects	adverse drug reaction reports ⓘ
cooperatesWith	European Medicines Agency ⓘ World Health Organization ⓘ other national medicines agencies ⓘ
country	Norway ⓘ
hasRole	competent authority for medicinal products in Norway ⓘ national regulatory authority for medicines in Norway ⓘ
headquartersLocation	Oslo ⓘ
issues	guidelines for healthcare professionals on medicine use ⓘ safety warnings about medicines ⓘ
jurisdiction	Norway ⓘ
languageOfWorkOrName	Norwegian language ⓘ surface form: Norwegian
nativeName	Norwegian Medicines Agency self-linksurface differs ⓘ surface form: Statens legemiddelverk
oversees	biological medicinal products ⓘ biosimilar medicines ⓘ generic medicines ⓘ over-the-counter medicines ⓘ prescription medicines ⓘ
parentOrganization	Ministry of Health and Care Services (Norway) ⓘ surface form: Ministry of Health and Care Services of Norway
participatesIn	European medicines regulatory authorities ⓘ surface form: European medicines regulatory network
performs	benefit-risk assessment of medicines ⓘ inspection of pharmaceutical manufacturers ⓘ inspection of wholesalers of medicines ⓘ
regulates	medical devices ⓘ medicines ⓘ pharmaceutical products ⓘ veterinary medicines ⓘ
responsibleFor	approval of medicines ⓘ control of pharmaceutical advertising ⓘ drug safety monitoring ⓘ efficacy of medicines ⓘ ensuring safe use of medicines ⓘ market authorisation of medicines ⓘ monitoring of medicines ⓘ pharmacovigilance ⓘ quality of medicines ⓘ regulation of clinical trials of medicines ⓘ safety of medicines ⓘ
sector	healthcare ⓘ pharmaceutical regulation ⓘ
subjectOf	Norwegian pharmaceutical policy ⓘ
typeOfOrganization	public sector agency ⓘ
website	https://www.legemiddelverket.no ⓘ

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: Norwegian Medicines Agency
Description of subject: The Norwegian Medicines Agency is Norway’s national regulatory authority responsible for the approval, monitoring, and safe use of medicines and related health products.

Referenced by (3)

Full triples — surface form annotated when it differs from this entity's canonical label.

Ministry of Health and Care Services (Norway) → oversees → Norwegian Medicines Agency ⓘ

HOD → oversees → Norwegian Medicines Agency ⓘ

Norwegian Medicines Agency → nativeName → Norwegian Medicines Agency self-linksurface differs ⓘ

this entity surface form: Statens legemiddelverk