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Volumn 64, Issue 5, 2010, Pages 537-542

Validation of pharmaceutical potency determinations by quantitative nuclear magnetic resonance spectrometry

Author keywords

Active pharmaceutical ingredients; Nuclear magnetic resonance spectroscopy; Q NMR; Quantitative NMR

Indexed keywords

INDUSTRIAL LABORATORIES; LABORATORIES; MAGNETIC RESONANCE SPECTROSCOPY; MAGNETISM; NUCLEAR MAGNETIC RESONANCE; RESONANCE; TOXICITY; TURNAROUND TIME;

EID: 77952729219     PISSN: 00037028     EISSN: None     Source Type: Journal    
DOI: 10.1366/000370210791211655     Document Type: Article
Times cited : (12)

References (17)
  • 1
    • 77952739750 scopus 로고    scopus 로고
    • The laboratory analyst's role in the drug development process
    • J. M Miller and J. B. Crowther, Eds. Wiley, New, York, Chap. 1
    • J. B. Crowther, W. Lauwers, S. Adusumalli, and P. Shenbagamurthi, "The Laboratory Analyst's Role in the Drug Development Process", in Analytical Chemistry in a GMP Environment, J. M. Miller and J. B. Crowther, Eds. (Wiley, New, York, 2000), Chap. 1, p. 3.
    • (2000) Analytical Chemistry in A GMP Environment , pp. 3
    • Crowther, J.B.1    Lauwers, W.2    Adusumalli, S.3    Shenbagamurthi, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.