European Medicines Agency (EMA)
GPTKB entity
Statements (57)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:regulations
|
| gptkbp:case_outcome |
marketing authorization applications
|
| gptkbp:collaborates_with |
gptkb:European_Commission
European Medicines Regulatory Network |
| gptkbp:conducts_research_on |
regulatory science
|
| gptkbp:coordinates |
inspections of manufacturing sites
|
| gptkbp:established |
gptkb:1995
|
| gptkbp:facilitates |
access to medicines
|
| gptkbp:function |
evaluation of medicinal products
|
| gptkbp:has_advisory_board |
scientific committees
|
| gptkbp:has_publications |
gptkb:educational_materials
annual reports newsletters research findings position papers webinars and events clinical trial results regulatory updates safety communications scientific opinions guidance documents assessment reports guidelines for stakeholders scientific advice reports |
| gptkbp:has_role |
pharmacovigilance
|
| gptkbp:headquarters |
gptkb:Amsterdam,_Netherlands
|
| https://www.w3.org/2000/01/rdf-schema#label |
European Medicines Agency (EMA)
|
| gptkbp:issues_reports_on |
annual activity report
|
| gptkbp:monitors |
safety of medicines
|
| gptkbp:operates_under |
gptkb:European_Union
|
| gptkbp:parent_organization |
gptkb:European_Union
|
| gptkbp:participates_in |
international regulatory cooperation
|
| gptkbp:promotes |
public health
|
| gptkbp:provides_guidance_on |
gptkb:European_Commission
gptkb:European_Parliament clinical trials post-marketing studies good clinical practice risk management plans good laboratory practice good manufacturing practice |
| gptkbp:provides_information_on |
patients and healthcare professionals
|
| gptkbp:provides_support_for |
orphan medicinal products
|
| gptkbp:provides_training_for |
regulatory professionals
|
| gptkbp:publishes |
guidelines for pharmaceutical companies
|
| gptkbp:responsible_for |
scientific evaluation of medicines
|
| gptkbp:stakeholders |
gptkb:healthcare_professionals
industry representatives patients research organizations regulatory authorities |
| gptkbp:supports |
research and development of medicines
|
| gptkbp:website |
www.ema.europa.eu
|
| gptkbp:works_with |
national competent authorities
|
| gptkbp:bfsParent |
gptkb:Sanofi
gptkb:Cure_Vac |
| gptkbp:bfsLayer |
4
|