9786202516365 - product quality review vs. continued process verification (pqr vs.cpv): a practical guide for pharmaceutical industries in adhering with regulatory compliance requirements di kumar, sanjeev (5 risultati)
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Da: moluna, Greven, Germaniamoluna
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EUR 29,02
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Kartoniert / Broschiert. Condizione: New.
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Da: preigu, Osnabrück, Germaniapreigu
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Taschenbuch. Condizione: Neu. Product Quality Review Vs. Continued Process Verification (PQR [.]) | A Practical Guide for Pharmaceutical Industries in adhering with Regulatory Compliance requirements | Sanjeev Kumar | Taschenbuch | Englisch | 2021 | LAP LAMBERT Academic Publishing | EAN 9786202516365 | Verantwortliche Person für… die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Product Quality Review and Continued Process Verification are the key essential documents through which a regulatory inspection normally begins in pharmaceutical industry, while evaluating the consistency and robustness of a produc…t or processes is not merely a regulatory requirement but important for a firm is to learn and introspect their product and process performance and whether manufacturing process including systems and sub-operations do functions in collaboration with each other to deliver sustainable quality products in servicing to mankind across the consumer(s) value chain. PQR & CPV are the documentational outcome not limited to manufacturing processes but mainly are the results of a robust QMS possess encompasses the organization structure, systems, processes, procedures, resources, operations, supply chain, Quality control, Quality Assurance function together to provide safe and quality medicines to deserving patients. With the crisp book on PQR/CPV, author put an effort to deliver a standardized framework in documenting PQR Vs. CPV program can benefit to pharmaceutical industries at large as well can add value to academia, pharmaceutical professionals. 72 pp. Englisch.
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Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Product Quality Review and Continued Process Verification are the key essential documents through which a regulatory inspection normally begins in pharmaceutical industry, while evaluating the consistency and robustness of a product or… processes is not merely a regulatory requirement but important for a firm is to learn and introspect their product and process performance and whether manufacturing process including systems and sub-operations do functions in collaboration with each other to deliver sustainable quality products in servicing to mankind across the consumer(s) value chain. PQR & CPV are the documentational outcome not limited to manufacturing processes but mainly are the results of a robust QMS possess encompasses the organization structure, systems, processes, procedures, resources, operations, supply chain, Quality control, Quality Assurance function together to provide safe and quality medicines to deserving patients. With the crisp book on PQR/CPV, author put an effort to deliver a standardized framework in documenting PQR Vs. CPV program can benefit to pharmaceutical industries at large as well can add value to academia, pharmaceutical professionals.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 72 pp. Englisch.
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 34,42
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Product Quality Review and Continued Process Verification are the key essential documents through which a regulatory inspection normally begins in pharmaceutical industry, while evaluating the consistency and robustness of a product or…processes is not merely a regulatory requirement but important for a firm is to learn and introspect their product and process performance and whether manufacturing process including systems and sub-operations do functions in collaboration with each other to deliver sustainable quality products in servicing to mankind across the consumer(s) value chain. PQR & CPV are the documentational outcome not limited to manufacturing processes but mainly are the results of a robust QMS possess encompasses the organization structure, systems, processes, procedures, resources, operations, supply chain, Quality control, Quality Assurance function together to provide safe and quality medicines to deserving patients. With the crisp book on PQR/CPV, author put an effort to deliver a standardized framework in documenting PQR Vs. CPV program can benefit to pharmaceutical industries at large as well can add value to academia, pharmaceutical professionals.
