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Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. The current good manufacturing practice (cGMP) and Food Drug Administration (FDA) Guidelines insist for adoption of sound methods of analysis with greater sensitivity and reproducibility. This thesis describes analytical methods developed for drug determination in pharmaceutical dosage forms and biological matrixes including Chromatography (RP-HPLC) and Hyphenated Techniques (LC-MS/MS). Methods have been developed for separation and quantification of selected drugs from categories like Antihypertensive, Antihyperlipidemic, Skeletal Muscle Relaxant, Non-Steroidal Anti-inflammatory Drug (NSAID), Antibiotic, Anticonvulsant, Antiviral, and Analeptic.
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Analytical Method Development by Liquid Chromatography: Development and Validation of Analytical Methods for the Assay of Selected Drugs in Pharmaceutical Dosage forms and Biological fluids
2011-10-25, LAP Lambert Academic Publishing
Paperback
in English
3844328696 9783844328691
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- Created November 25, 2011
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August 22, 2020 | Edited by ISBNbot2 | normalize ISBN |
August 9, 2012 | Edited by VacuumBot | Updated format 'paperback' to 'Paperback' |
November 25, 2011 | Edited by 59.99.16.180 | Added new cover |
November 25, 2011 | Edited by 59.99.16.180 | Added new cover |
November 25, 2011 | Created by 59.99.16.180 | Added new book. |