Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q7240891> ?p ?o }
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- Q7240891 subject Q8463108.
- Q7240891 subject Q8760205.
- Q7240891 abstract "The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA) to collect fees from drug manufacturers to fund the new drug approval process. The Act provided that the FDA was entitled to collect a substantial application fee from drug manufacturers at the time a New Drug Application (NDA) or Biologics License Application (BLA) was submitted, with those funds designated for use only in Center for Drug Evaluation and Research (CDER) or Center for Biologics Evaluation and Research (CBER) drug approval activities. In order to continue collecting such fees, the FDA is required to meet certain performance benchmarks, primarily related to the speed of certain activities within the NDA review process.".
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- Q7240891 wikiPageExternalLink STATUTE-106-Pg4491.pdf.
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- Q7240891 wikiPageWikiLink Q8463108.
- Q7240891 wikiPageWikiLink Q8760205.
- Q7240891 wikiPageWikiLink Q929833.
- Q7240891 comment "The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA) to collect fees from drug manufacturers to fund the new drug approval process.".
- Q7240891 label "Prescription Drug User Fee Act".