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.
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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 publication like books/ review/research articles. Dr. S.D. Barhate, M.Ph., Ph.D., Pharmacist, Principal at SSJIPER, Jamner, MH, India.
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Anbieter: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Deutschland
Taschenbuch. Zustand: 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. Bestandsnummer des Verkäufers 9786202012782
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Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
Paperback. Zustand: Brand New. 80 pages. 8.66x5.91x0.19 inches. In Stock. Bestandsnummer des Verkäufers zk6202012781
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Zustand: 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 publication like books/ review/research. Bestandsnummer des Verkäufers 165763587
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Taschenbuch. Zustand: 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. Bestandsnummer des Verkäufers 9786202012782
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Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: 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 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. Bestandsnummer des Verkäufers 9786202012782
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Anbieter: preigu, Osnabrück, Deutschland
Taschenbuch. Zustand: 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]preigu[dot]de | Anbieter: preigu. Bestandsnummer des Verkäufers 109642388
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