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Product Quality Review Vs. Continued Process Verification (PQR Vs.CPV): A Practical Guide for Pharmaceutical Industries in adhering with Regulatory Compliance requirements - Couverture souple
Synopsis
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.
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- ÉditeurLAP LAMBERT Academic Publishing
- Date d'édition2021
- ISBN 10 6202516364
- ISBN 13 9786202516365
- ReliureBroché
- Langueanglais
- Nombre de pages72
- Coordonnées du fabricantnon disponible
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Product Quality Review Vs. Continued Process Verification (PQR Vs.CPV)
Edité par
LAP LAMBERT Academic Publishing, 2021
ISBN 10 : 6202516364
ISBN 13 : 9786202516365
Neuf
Couverture souple
Vendeur : moluna, Greven, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Etat : New. N° de réf. du vendeur 536000264
Quantité disponible : Plus de 20 disponibles
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Product Quality Review Vs. Continued Process Verification (PQR Vs.CPV)
Edité par
LAP LAMBERT Academic Publishing Nov 2021, 2021
ISBN 10 : 6202516364
ISBN 13 : 9786202516365
Neuf
Taschenbuch
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Taschenbuch. Etat : 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 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. 72 pp. Englisch. N° de réf. du vendeur 9786202516365
Quantité disponible : 2 disponible(s)
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Product Quality Review Vs. Continued Process Verification (PQR Vs.CPV) : A Practical Guide for Pharmaceutical Industries in adhering with Regulatory Compliance requirements
Edité par
LAP LAMBERT Academic Publishing, 2021
ISBN 10 : 6202516364
ISBN 13 : 9786202516365
Neuf
Taschenbuch
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Taschenbuch. Etat : 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. N° de réf. du vendeur 9786202516365
Quantité disponible : 1 disponible(s)
Image fournie par le vendeur
Product Quality Review Vs. Continued Process Verification (PQR Vs.CPV)
Edité par
LAP LAMBERT Academic Publishing Nov 2021, 2021
ISBN 10 : 6202516364
ISBN 13 : 9786202516365
Neuf
Taschenbuch
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Évaluation du vendeur 5 sur 5 étoiles
Taschenbuch. Etat : Neu. 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.Books on Demand GmbH, Überseering 33, 22297 Hamburg 72 pp. Englisch. N° de réf. du vendeur 9786202516365
Quantité disponible : 2 disponible(s)