9786202012782 - fdc tablet : quality development & pharmaceutical process validation de patil, shital s.; barhate, s. d.; upasani, manali s. (6 resultados)

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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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Paperback. Condición: Brand New. 80 pages. 8.66x5.91x0.19 inches. In Stock.

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Librería: preigu, Osnabrück, Alemaniapreigu
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Taschenbuch. Condición: Neu. FDC Tablet : Quality Development & Pharmaceutical Process Validation | Shital S. Patil (u. a.) | Taschenbuch | 80 S. | Englisch | 2017 | LAP LAMBERT Academic Publishing | EAN 9786202012782 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]pre…igu[dot]de | Anbieter: preigu.

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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This is book (part 01), based on introduction, of the project entitled 'Quality development and Pharmaceutical Process Validation of critical steps involved in manufacturing of 2-FDC tablets'. Introduction is most important part of…any project. This study involves validating process variables of this product to show that process was under control the study was conducted on three validation batches, which includes validation of critical steps such as dry mixing, granulation, drying, lubrication, compression, coating overall manufacturing process was concluded as validated at the parameters mentioned above as per BMR and BMR.The raw materials required for these validation batches were procured from approved sources and were taken up for manufacturing after testing and release by Quality control. The raw materials were dispensed as per Standard Operating Procedure. The data has been compiled in such a way to feel it as 'ready to use'. This book is not usual type book; we have tried to make it more reader friendly. 80 pp. Englisch.

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Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Patil Shital S.Shital S. Patil, M.Pharm (QA), Pharmacist, Asst Prof at SSJIPER, Jamner, India, Authored review/research articles. Manali S. Upasani, M.Pharm (QA), Pharmacist, Authored versatile publicat…ion like books/ review/research.

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Librería: buchversandmimpf2000, Emtmannsberg, BAYE, Alemaniabuchversandmimpf2000
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Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This is book (part 01), based on introduction, of the project entitled ¿Quality development and Pharmaceutical Process Validation of critical steps involved in manufacturing of 2-FDC tablets¿. Introduction is most important part of any…project. This study involves validating process variables of this product to show that process was under control the study was conducted on three validation batches, which includes validation of critical steps such as dry mixing, granulation, drying, lubrication, compression, coating overall manufacturing process was concluded as validated at the parameters mentioned above as per BMR and BMR.The raw materials required for these validation batches were procured from approved sources and were taken up for manufacturing after testing and release by Quality control. The raw materials were dispensed as per Standard Operating Procedure. The data has been compiled in such a way to feel it as ¿ready to use¿. This book is not usual type book; we have tried to make it more reader friendly.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 80 pp. Englisch.

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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - This is book (part 01), based on introduction, of the project entitled 'Quality development and Pharmaceutical Process Validation of critical steps involved in manufacturing of 2-FDC tablets'. Introduction is most important part of any p…roject. This study involves validating process variables of this product to show that process was under control the study was conducted on three validation batches, which includes validation of critical steps such as dry mixing, granulation, drying, lubrication, compression, coating overall manufacturing process was concluded as validated at the parameters mentioned above as per BMR and BMR.The raw materials required for these validation batches were procured from approved sources and were taken up for manufacturing after testing and release by Quality control. The raw materials were dispensed as per Standard Operating Procedure. The data has been compiled in such a way to feel it as 'ready to use'. This book is not usual type book; we have tried to make it more reader friendly.