Development validation analytical method von vaishnani bhavinkumar (6 Ergebnisse)
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Taschenbuch. Zustand: Neu. Development and Validation of Analytical Method for lower dosage form | Different Spectrophotometric and Chromatographic methods for Quantification of Rasagiline | Bhavinkumar Vaishnani | Taschenbuch | 188 S. | Englisch | 2011 | LAP LAMBERT Academic Publishing | EAN 9783844384284 | Verantwortliche Pers…on für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.
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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -To meet the emerging challenges of 21st century, the number of drugs introduced into the global pharmaceutical market is increasing every year. The focus on research and development of the drug molecule is to introduce either new enti…ties or partial structural modification of the existing one to improve its potency and/or to reduce its adverse effect. Very often there is a time lag from the date of introduction of a drug into the market to the date of its inclusion in pharmacopoeias. This happens because of the possible uncertainties in the continuous and wider usage of these drugs, reports of new toxicities (resulting in their withdrawal from the market), development of patient resistance and introduction of better drugs by the competitors. Under these conditions, standard analytical procedures for these drugs may not be available in the pharmacopoeias. The analysis of high-potency, low-strength solid oral dosage forms poses a number of analytical challenges that can impact potency, purity and dissolution testing of the dosage form. 188 pp. Englisch.
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Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Vaishnani BhavinkumarBhavinkumar K. Vaishnani, M.Pharmacy (Quality Assurance)fromRajiv Gandhi University of Health Science, Bangalore, INDIATo meet the emerging challenges of 21st century, thenumber of dr…ugs introduced into the g.
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Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -To meet the emerging challenges of 21st century, thenumber of drugs introduced into the globalpharmaceutical market is increasing every year. Thefocus on research and development of the drugmolecule is to introduce either new entities orp…artial structural modification of the existing oneto improve its potency and/or to reduce its adverseeffect. Very often there is a time lag from the dateof introduction of a drug into the market to the dateof its inclusion in pharmacopoeias. This happensbecause of the possible uncertainties in thecontinuous and wider usage of these drugs, reports ofnew toxicities (resulting in their withdrawal fromthe market), development of patient resistance andintroduction of better drugs by the competitors.Under these conditions, standard analyticalprocedures for these drugs may not be available inthe pharmacopoeias.The analysis of high-potency, low-strength solid oraldosage forms poses a number of analytical challengesthat can impact potency, purity and dissolutiontesting of the dosage form.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 188 pp. Englisch.
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - To meet the emerging challenges of 21st century, the number of drugs introduced into the global pharmaceutical market is increasing every year. The focus on research and development of the drug molecule is to introduce either new entities…or partial structural modification of the existing one to improve its potency and/or to reduce its adverse effect. Very often there is a time lag from the date of introduction of a drug into the market to the date of its inclusion in pharmacopoeias. This happens because of the possible uncertainties in the continuous and wider usage of these drugs, reports of new toxicities (resulting in their withdrawal from the market), development of patient resistance and introduction of better drugs by the competitors. Under these conditions, standard analytical procedures for these drugs may not be available in the pharmacopoeias. The analysis of high-potency, low-strength solid oral dosage forms poses a number of analytical challenges that can impact potency, purity and dissolution testing of the dosage form.
