Browse Wiki & Semantic Web

Jump to: navigation, search
Http://dbpedia.org/resource/Marketing Authorisation Application
  This page has no properties.
hide properties that link here 
  No properties link to this page.
 
http://dbpedia.org/resource/Marketing_Authorisation_Application
http://dbpedia.org/ontology/abstract Marketing Authorisation Application (MAA) Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking marketing authorisation, that is permission to bring a medicinal product (for example, a new medicine or generic medicine) to the market. MAA is part of the official procedure before the Medicines and Healthcare products Regulatory Agency in the United Kingdom and the Committee for Medicinal Products for Human Use of the European Medicines Agency, a specialised agency of the European Commission. In the United States, the equivalent process is called New Drug Application.nt process is called New Drug Application.
http://dbpedia.org/ontology/wikiPageID 23226758
http://dbpedia.org/ontology/wikiPageLength 898
http://dbpedia.org/ontology/wikiPageRevisionID 949642401
http://dbpedia.org/ontology/wikiPageWikiLink http://dbpedia.org/resource/United_Kingdom + , http://dbpedia.org/resource/Medicines_and_Healthcare_products_Regulatory_Agency + , http://dbpedia.org/resource/Category:Drug_safety + , http://dbpedia.org/resource/United_States + , http://dbpedia.org/resource/Medicinal_product + , http://dbpedia.org/resource/New_Drug_Application + , http://dbpedia.org/resource/Marketing_authorisation + , http://dbpedia.org/resource/Committee_for_Medicinal_Products_for_Human_Use + , http://dbpedia.org/resource/European_Commission + , http://dbpedia.org/resource/European_Medicines_Agency +
http://dbpedia.org/property/wikiPageUsesTemplate http://dbpedia.org/resource/Template:Reflist +
http://purl.org/dc/terms/subject http://dbpedia.org/resource/Category:Drug_safety +
http://www.w3.org/ns/prov#wasDerivedFrom http://en.wikipedia.org/wiki/Marketing_Authorisation_Application?oldid=949642401&ns=0 +
http://xmlns.com/foaf/0.1/isPrimaryTopicOf http://en.wikipedia.org/wiki/Marketing_Authorisation_Application +
owl:sameAs https://global.dbpedia.org/id/4rSkT + , http://www.wikidata.org/entity/Q6770873 + , http://dbpedia.org/resource/Marketing_Authorisation_Application +
rdfs:comment Marketing Authorisation Application (MAA) Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking marketing authorisation, that is permission to bring a medicinal product (for example, a new medicine or generic medicine) to the market. MAA is part of the official procedure before the Medicines and Healthcare products Regulatory Agency in the United Kingdom and the Committee for Medicinal Products for Human Use of the European Medicines Agency, a specialised agency of the European Commission. In the United States, the equivalent process is called New Drug Application.nt process is called New Drug Application.
rdfs:label Marketing Authorisation Application
hide properties that link here 
http://dbpedia.org/resource/Marketing_Authorization_Application + http://dbpedia.org/ontology/wikiPageRedirects
http://dbpedia.org/resource/European_Directorate_for_the_Quality_of_Medicines_&_HealthCare + , http://dbpedia.org/resource/Marketing_Authorization_Application + , http://dbpedia.org/resource/Groundwater_contamination_by_pharmaceuticals + , http://dbpedia.org/resource/Marketing_authorisation_application + http://dbpedia.org/ontology/wikiPageWikiLink
http://en.wikipedia.org/wiki/Marketing_Authorisation_Application + http://xmlns.com/foaf/0.1/primaryTopic
http://dbpedia.org/resource/Marketing_Authorisation_Application + owl:sameAs
 

 

Enter the name of the page to start semantic browsing from.