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Volumn 83, Issue 3, 2008, Pages 393-395

Should herbal medicines be regulated as drugs?

Author keywords

[No Author keywords available]

Indexed keywords

ASTRINGENT AGENT; ATORVASTATIN; DIGOXIN; EMOLLIENT AGENT; EPHEDRA EXTRACT; HAMAMELIS EXTRACT; HERBACEOUS AGENT; ISPAGULA; LAXATIVE; MORPHINE; NON PRESCRIPTION DRUG; SENNOSIDE;

EID: 39449084058     PISSN: 00099236     EISSN: 15326535     Source Type: Journal    
DOI: 10.1038/sj.clpt.6100480     Document Type: Short Survey
Times cited : (8)

References (19)
  • 1
    • 39449128141 scopus 로고    scopus 로고
    • Title 21 United States Code, Section 343(r)(6)(B, 21 U.S.C. 343(r)(6)B
    • Title 21 United States Code, Section 343(r)(6)(B) [21 U.S.C. 343(r)(6)(B)].
  • 4
    • 39449117859 scopus 로고    scopus 로고
    • U.S. Court of Appeals Tenth Circuit; 17 August 2006; No. 05-1541.
    • U.S. Court of Appeals Tenth Circuit; 17 August 2006; No. 05-1541.
  • 5
    • 39449139788 scopus 로고    scopus 로고
    • U.S. Court of Appeals Third Circuit; 7 February 2006; No. 04-4481.
    • U.S. Court of Appeals Third Circuit; 7 February 2006; No. 04-4481.
  • 7
    • 39449085990 scopus 로고    scopus 로고
    • Title 21 Code of Federal Regulations, Section 190.6(b)(4) [21 CFR 190.6(b)(4)].
    • Title 21 Code of Federal Regulations, Section 190.6(b)(4) [21 CFR 190.6(b)(4)].
  • 8
    • 39449130024 scopus 로고    scopus 로고
    • 110th Congress; S.A. 1022 to S. 1082; 2 May 2007.
    • 110th Congress; S.A. 1022 to S. 1082; 2 May 2007.
  • 9
    • 39449135486 scopus 로고    scopus 로고
    • Stupak, B., chairman, Oversight and Investigations Subcommittee, US House of Representatives Committee on Energy and Commerce. FDA Foreign Drug Inspection Program: A System at Risk 〈http://energycommerce.house.gov/ Subcommittees/OI-Stupak/110107.OI.FDA.drugsafety.pdf〉 (1 November 2007).
    • Stupak, B., chairman, Oversight and Investigations Subcommittee, US House of Representatives Committee on Energy and Commerce. FDA Foreign Drug Inspection Program: A System at Risk 〈http://energycommerce.house.gov/ Subcommittees/OI-Stupak/110107.OI.FDA.drugsafety.pdf〉 (1 November 2007).
  • 12
    • 39449131293 scopus 로고    scopus 로고
    • US Food and Drug Administration. 21 CFR Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Final Rule. Federal Register 72, 34752-39958 (25 June 2007).
    • US Food and Drug Administration. 21 CFR Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Final Rule. Federal Register 72, 34752-39958 (25 June 2007).
  • 13
    • 39449093821 scopus 로고    scopus 로고
    • 21 CFR 111.70(b)3
    • 21 CFR 111.70(b)(3).
  • 14
    • 39449133518 scopus 로고    scopus 로고
    • US Food and Drug Administration. 21 CFR Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Final Rule. Federal Register 72, 34782 (25 June 2007).
    • US Food and Drug Administration. 21 CFR Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Final Rule. Federal Register 72, 34782 (25 June 2007).
  • 15
    • 39449097126 scopus 로고    scopus 로고
    • 21 CFR 111.70 and 111.75.
    • 21 CFR 111.70 and 111.75.
  • 16
    • 39449097724 scopus 로고    scopus 로고
    • 21 CFR 111, subpart F.
    • 21 CFR 111, subpart F.
  • 17
    • 39449124195 scopus 로고    scopus 로고
    • 21 CFR 111.610
    • 21 CFR 111.610.
  • 18
    • 39449100440 scopus 로고    scopus 로고
    • 21 CFR 101.36 and relevant sections of 21 CFR 101.4 and 101.9.
    • 21 CFR 101.36 and relevant sections of 21 CFR 101.4 and 101.9.
  • 19
    • 39449095057 scopus 로고    scopus 로고
    • 21 CFR 101.93
    • 21 CFR 101.93.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.