Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q638880> ?p ?o }
Showing triples 1 to 19 of
19
with 100 triples per page.
- Q638880 subject Q7056690.
- Q638880 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.".
- Q638880 wikiPageExternalLink 013402.pdf.
- Q638880 wikiPageExternalLink download.
- Q638880 wikiPageExternalLink dmf.htm.
- Q638880 wikiPageExternalLink index.html.
- Q638880 wikiPageWikiLink Q1116233.
- Q638880 wikiPageWikiLink Q12140.
- Q638880 wikiPageWikiLink Q1292017.
- Q638880 wikiPageWikiLink Q131257.
- Q638880 wikiPageWikiLink Q1368197.
- Q638880 wikiPageWikiLink Q204711.
- Q638880 wikiPageWikiLink Q4664417.
- Q638880 wikiPageWikiLink Q6060674.
- Q638880 wikiPageWikiLink Q7056690.
- Q638880 wikiPageWikiLink Q718608.
- Q638880 wikiPageWikiLink Q912807.
- Q638880 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.".
- Q638880 label "Drug Master File".