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Volumn 21, Issue 4, 2009, Pages 603-618

Development and validation of a high-performance liquid chromatographic method for analysis of nimesulide residues on manufacturing equipment surfaces

Author keywords

Cleaning validation; Nimesulide; Residues on surfaces; Swab analysis

Indexed keywords


EID: 73249116553     PISSN: 12332356     EISSN: 20835736     Source Type: Journal    
DOI: 10.1556/AChrom.21.2009.4.7     Document Type: Article
Times cited : (5)

References (21)
  • 1
    • 0003548169 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration available at: (accessed 27/10/2009)
    • Guide to Inspections Validation of Cleaning Processes, U.S. Food and Drug Administration available at: http://www.fda.gov/ICECI/Inspections/ InspectionGuides/ ucm074922.htm (accessed 27/10/2009)
    • Guide to Inspections Validation of Cleaning Processes
  • 2
    • 73249133390 scopus 로고    scopus 로고
    • Supplementary guidelines on good manufacturing practices (GMP): Validation
    • World Health Organization, available at: (accessed 10 Oct, 2009)
    • World Health Organization, Supplementary guidelines on good manufacturing practices (GMP): Validation, Working document QAS/03.055/Rev.2, pp 24-33, available at: http://www.who.int/medicines/services/expertcommittees/pharmprep/ Validation-QAS-055-Rev2combined.pdf (accessed 10 Oct, 2009)
    • Working Document QAS/03.055/Rev.2 , pp. 24-33
  • 3
    • 27644555907 scopus 로고    scopus 로고
    • Active Pharmaceutical Ingredients Committee (APIC), available at: (accessed 10 Oct, 2009)
    • Guidance on aspects of cleaning validation in active pharmaceutical ingredient plants, Active Pharmaceutical Ingredients Committee (APIC), pp 1-56, available at: http://apic.cefic.org/pub/pub-cleaning-validation.pdf (accessed 10 Oct, 2009)
    • Guidance on Aspects of Cleaning Validation in Active Pharmaceutical Ingredient Plants , pp. 1-56


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.