Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Drug_Master_File> ?p ?o }
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- Drug_Master_File abstract "Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document provides the regulatory authority with confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs. Typically, a drug master file is filed when two or more firms work in partnership on developing or manufacturing a drug product. The DMF filing allows a firm to protect its intellectual property from its partner while complying with regulatory requirements for disclosure of processing details.".
- Drug_Master_File wikiPageExternalLink 013402.pdf.
- Drug_Master_File wikiPageExternalLink download.
- Drug_Master_File wikiPageExternalLink dmf.htm.
- Drug_Master_File wikiPageExternalLink index.html.
- Drug_Master_File wikiPageID "8819015".
- Drug_Master_File wikiPageLength "35676".
- Drug_Master_File wikiPageOutDegree "12".
- Drug_Master_File wikiPageRevisionID "700472379".
- Drug_Master_File wikiPageWikiLink Abbreviated_New_Drug_Application.
- Drug_Master_File wikiPageWikiLink Active_ingredient.
- Drug_Master_File wikiPageWikiLink Category:Pharmaceutical_industry.
- Drug_Master_File wikiPageWikiLink Certified_translation.
- Drug_Master_File wikiPageWikiLink Common_Technical_Document.
- Drug_Master_File wikiPageWikiLink Dosage_form.
- Drug_Master_File wikiPageWikiLink Food_and_Drug_Administration.
- Drug_Master_File wikiPageWikiLink Good_manufacturing_practice.
- Drug_Master_File wikiPageWikiLink Intellectual_property.
- Drug_Master_File wikiPageWikiLink Investigational_New_Drug.
- Drug_Master_File wikiPageWikiLink New_drug_application.
- Drug_Master_File wikiPageWikiLink Pharmaceutical_drug.
- Drug_Master_File wikiPageWikiLinkText "Drug Master File".
- Drug_Master_File wikiPageWikiLinkText "Drug Master file".
- Drug_Master_File wikiPageUsesTemplate Template:More_footnotes.
- Drug_Master_File wikiPageUsesTemplate Template:Multiple_issues.
- Drug_Master_File wikiPageUsesTemplate Template:Reflist.
- Drug_Master_File wikiPageUsesTemplate Template:Underlinked.
- Drug_Master_File subject Category:Pharmaceutical_industry.
- Drug_Master_File hypernym Document.
- Drug_Master_File type Book.
- Drug_Master_File type Industry.
- Drug_Master_File type Pharmaceutic.
- Drug_Master_File comment "Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document provides the regulatory authority with confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.".
- Drug_Master_File label "Drug Master File".
- Drug_Master_File sameAs Q638880.
- Drug_Master_File sameAs Drug_Master_File.
- Drug_Master_File sameAs Drug_Master_File.
- Drug_Master_File sameAs Drug_Master_File.
- Drug_Master_File sameAs ドラッグマスターファイル.
- Drug_Master_File sameAs m.027kvld.
- Drug_Master_File sameAs Q638880.
- Drug_Master_File wasDerivedFrom Drug_Master_File?oldid=700472379.
- Drug_Master_File isPrimaryTopicOf Drug_Master_File.