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pro vyhledávání: '"Julie J. Tomlinson"'
Autor:
Julie J. Tomlinson
Publikováno v:
The Journal of Automatic Chemistry
Bioanalytical automation expanded at Glaxo Inc. from 1987 to 1991 by cycling through periods of justification, planning, implementation, obstacle-jumping and success, which justified continued cycling. In 1990 it became evident that the technology an
Autor:
Julie J. Tomlinson
Publisher Summary Laboratory automation is widely used in the pharmaceutical industry to support quality control, nonclinical and clinical drug development, and drug discovery. Analytical applications for which automation is commonly utilized include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0740f639103bb39a44eb103ac56d4620
https://doi.org/10.1016/s1464-3456(96)80010-x
https://doi.org/10.1016/s1464-3456(96)80010-x
Publikováno v:
Biomedical chromatography : BMC. 6(6)
A fully automated assay for the analysis of ranitidine in serum and plasma, with and without an internal standard, was validated. It utilizes robotic solid phase extraction with on-line high performance liquid chromatographic (HPLC) analysis. The rug
Autor:
Paul Morris, R., Tomlinson, Julie J.
Publikováno v:
IEEE Transactions on Consumer Electronics; Aug2008, Vol. 54 Issue 3, p1252-1258, 7p, 7 Diagrams
Publikováno v:
Journal of Automated Methods & Management in Chemistry; 1998, Vol. 20 Issue 2, p31-66, 36p
Autor:
Tomlinson, Julie J.
Publikováno v:
Journal of Automated Methods & Management in Chemistry; 1992, Vol. 14 Issue 2, p47-50, 4p
Autor:
CURRAN, DAVID J.
Publikováno v:
Journal of Automated Methods & Management in Chemistry; 1991, Vol. 13 Issue 6, p243-266, 24p
Publikováno v:
Biomedical Chromatography; Nov1992, Vol. 6 Issue 6, p311-316, 6p
Autor:
Tomlinson, Julie J., Butler, Brent T., Frezza, Joan, Harris, Cole O., Smith, Albert A., Knight, W. Blaine
Publikováno v:
Journal of Automated Methods & Management in Chemistry; 1998, Vol. 20 Issue 3, p83-85, 3p
The need to validate an analytical or bioanalytical method is encountered by analysts in the pharmaceutical industry on an almost daily basis, because adequately validated methods are a necessity for approvable regulatory filings. What constitutes a