Synopsis
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.
"synopsis" may belong to another edition of this title.
About the Author
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.
"About this title" may belong to another edition of this title.
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FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing Aug 2017, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
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Taschenbuch. Condition: 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. Seller Inventory # 9786202012782
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FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
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Paperback. Condition: Brand New. 80 pages. 8.66x5.91x0.19 inches. In Stock. Seller Inventory # zk6202012781
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FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
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Condition: 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. Seller Inventory # 165763587
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FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing Aug 2017, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
New
Taschenbuch
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germany
Seller rating 5 out of 5 stars
Taschenbuch. Condition: 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. Seller Inventory # 9786202012782
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FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
New
Taschenbuch
Seller: AHA-BUCH GmbH, Einbeck, Germany
Seller rating 5 out of 5 stars
Taschenbuch. Condition: 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. Seller Inventory # 9786202012782
Seller Image
FDC Tablet : Quality Development & Pharmaceutical Process Validation
Published by
LAP LAMBERT Academic Publishing, 2017
ISBN 10: 6202012781
ISBN 13: 9786202012782
New
Taschenbuch
Seller: preigu, Osnabrück, Germany
Seller rating 5 out of 5 stars
Taschenbuch. Condition: 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. Seller Inventory # 109642388