Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis.
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Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis.
Working as Assistant Professor in MMCP, Mullana. Passed B. Pharmacy from GGSCOP, Yamunanagar; M Pharmacy from GJUS&T, Hisar.Teaching experience of 5 yrs. More than 15 national/international publications and participated in many conferences.Won best podium presentation in ICPS-2014.Guided many research students.Member of various academic association
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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis. 88 pp. Englisch. Nº de ref. del artículo: 9783659564253
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Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Chaudhary JasmineWorking as Assistant Professor in MMCP, Mullana. Passed B. Pharmacy from GGSCOP, Yamunanagar M Pharmacy from GJUS&T, Hisar.Teaching experience of 5 yrs. More than 15 national/international publications and participa. Nº de ref. del artículo: 5165058
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Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 88 pp. Englisch. Nº de ref. del artículo: 9783659564253
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Taschenbuch. Condición: Neu. Novel RP-HPLC Method for determination of pregabalin in capsule form | Jasmine Chaudhary (u. a.) | Taschenbuch | 88 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659564253 | Verantwortliche Person für die EU: OmniScriptum GmbH & Co. KG, Bahnhofstr. 28, 66111 Saarbrücken, info[at]akademikerverlag[dot]de | Anbieter: preigu. Nº de ref. del artículo: 105184319
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