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Volumn 16, Issue 4, 2008, Pages 67-85

Drug patent live and generic competition: Analysis of new molecular entities approved by the FDA between 1980 and 1999

Author keywords

Drug exclusivity; Drug patents; New molecular entities

Indexed keywords

GENERIC DRUG; MOLECULAR THERAPY AGENT; NEW DRUG; ORPHAN DRUG;

EID: 66249084667     PISSN: 15385698     EISSN: 15385396     Source Type: Journal    
DOI: 10.1080/15385690801963530     Document Type: Article
Times cited : (6)

References (16)
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    • Grabowski, H.G., and J.M. Vernon. 1996. Longer patents for increased generic competition in the US. TheWaxman-Hatch Act after one decade. Pharmacoeconomics 10(Suppl. no. 2): 110-123
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  • 8
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    • Heinrich, J. 2001. Pediatric drug research: Substantial increase in studies of drugs for children, but some challenges remain. Testimony before the committee on health, education, labor and pensions,U.S. Senate.Washington, DC:United StatesGeneral Accounting Office.
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    • Measuring the pace of new drug development in the user fee era
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    • (Advertisement)
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    • U.S. Food and Drug Administration. 2001. The pediatric exclusivity provision. Status report to Congress. Washington, DC: U.S. Food and Drug Administration. http://www.fda.gov/cder/pediatric/reportcong01.pdf.
    • (2001) The Pediatric Exclusivity Provision. Status Report to Congress


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.