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Volumn 551, Issue 1-2, 2005, Pages 159-167

Validation of LC-MS electrospray ionisation method for quantitation of haloperidol in human plasma and its application to bioequivalence study

Author keywords

Bioequivalence; Haloperidol; Method validation

Indexed keywords

AMMONIUM COMPOUNDS; BODY FLUIDS; CONCENTRATION (PROCESS); EXTRACTION; IONIZATION; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PLASMAS;

EID: 25844477027     PISSN: 00032670     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aca.2005.07.046     Document Type: Article
Times cited : (15)

References (20)
  • 18
    • 0003484310 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for veterinary Medicine (CVM) May BP.
    • Guidance for industry, Bioanalytical method validation. US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for veterinary Medicine (CVM) May 2001 BP. Website: http://www.fda.gov/cder/guidance/index.htm.
    • (2001) Guidance for Industry, Bioanalytical Method Validation
  • 19
    • 39549088409 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER)
    • FDA Guidance for Industry, Biaoavaliability Studies for Orally Administered Drug - Products-General Considerations, US Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER) 2000. Website: http://www.fda.gov/cder/guidance/index.htm.
    • (2000) Biaoavaliability Studies for Orally Administered Drug - Products-General Considerations
  • 20
    • 0003922012 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER)
    • FDA Guidance for Industry, Statistical Approaches to Establishing Bioequivalence, US Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER) 2001. Website: http://www.fda.gov/cder/guidance/index.htm
    • (2001) Statistical Approaches to Establishing Bioequivalence


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.