Paperback. Zustand: Good. No Jacket. Former library book; Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less.
Anbieter: Vedams eBooks (P) Ltd, New Delhi, Indien
Hardcover. Zustand: As New. 2nd Edition. Contents Foreword. Preface. Acknowledgements. List of abbreviations. Introduction. Part I 1. Regulatory requirements for pharmaceutical plants. 2. Project management. 3. Pharmaceutical validation. Part II 4. Pharmaceutical facility design. 5. Support Serv 266 pp.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 49,05
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 55,39
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Verlag: PharmaMed Press, 2018
ISBN 10: 9387593061 ISBN 13: 9789387593060
Anbieter: Vedams eBooks (P) Ltd, New Delhi, Indien
Soft cover. Zustand: As New. Contents Foreword. Preface. Acknowledgements. Introduction. 1. Personnel. 2. Surroundings buildings and facilities. 3. Equipment. 4. Materials management. 5. Quality management. 6. Manufacturing operations and control. 7. Documentation and records. 8. Pharmaceutical validation. 9. Outsourcing. 10. Post operational activities. 11. Sterile pharmaceutical products. 12. Site and plant security. 13. Safety and environmental protection. 14. Good pharmaceutical wholesaling practices. 15. Pharmaceutical audit. Glossary. Bibliography. Index. Indian Pharmaceutical Industry is becoming global at high pace. This resulted in high pressure on the industry for quality products and practices. Thus cGMP has acclaimed key position. Practicing cGMP requires clear understanding at conceptual and implementation level and that too at shop floor and middle management level. This book is written in simple and easy to implement manner. Salient features All current issues of cGMP demanded by regulatory authorities like W.H.O. M.H.R.A. T.G.A. U.S.F.D.A. and also Indian F.D.A. are fully discussed profusely referenced and thoroughly illustrated in simple and easy to understand language. Covers other important topics like plant site security environmental issues distribution of products and preparing for the regulatory audits etc. 798 pp.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 68,97
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 68,97
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 73,50
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
EUR 84,70
Anzahl: 1 verfügbar
In den Warenkorbhardcover. Zustand: Very Good. Pharmaceutical Plant Administration This book is in very good condition and will be shipped within 24 hours of ordering. The cover may have some limited signs of wear but the pages are clean, intact and the spine remains undamaged. This book has clearly been well maintained and looked after thus far. Money back guarantee if you are not satisfied. See all our books here, order more than 1 book and get discounted shipping. .
EUR 84,70
Anzahl: 1 verfügbar
In den Warenkorbhardcover. Zustand: Very Good. Shipped within 24 hours from our UK warehouse. Clean, undamaged book with no damage to pages and minimal wear to the cover. Spine still tight, in very good condition. Remember if you are not happy, you are covered by our 100% money back guarantee.
Sprache: Englisch
Verlag: Springer Verlag, Singapore, 2024
ISBN 10: 9819992702 ISBN 13: 9789819992706
Anbieter: PBShop.store UK, Fairford, GLOS, Vereinigtes Königreich
EUR 94,08
Anzahl: 1 verfügbar
In den WarenkorbHRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Sprache: Englisch
Verlag: Springer Verlag, Singapore, 2024
ISBN 10: 9819992702 ISBN 13: 9789819992706
Anbieter: PBShop.store US, Wood Dale, IL, USA
HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
EUR 53,00
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Über den AutorrnrnDr. Manohar A. Potdar, M. Pharm (BITS Pilani), Ph.D. (Production Management) USA was a professor emeritus of Pharmaceutical Sciences at Poona College of Pharmacy, Barati Vidyapeeth University, Pune, India. He taught Under.
Anbieter: Majestic Books, Hounslow, Vereinigtes Königreich
EUR 98,82
Anzahl: 1 verfügbar
In den WarenkorbZustand: New.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 111,28
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
EUR 73,98
Anzahl: Mehr als 20 verfügbar
In den WarenkorbGebunden. Zustand: New. Über den AutorrnrnDr. Manohar A. Potdar, M.Pharm (BITS Pilani), Ph.D. (Production Management) USA, Currently President Technical, Doshi Consultants Pvt. Ltd., Pharmaceutical Plant Design and Validation Consultants, was a professor emeritus .
EUR 73,98
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Über den AutorrnrnDr. Manohar A. Potdar, M.Pharm (BITS Pilani), Ph.D. (Production Management) USA, Currently President Technical, Doshi Consultants Pvt. Ltd., Pharmaceutical Plant Design and Validation Consultants, was a professor emeritus .
EUR 78,75
Anzahl: Mehr als 20 verfügbar
In den WarenkorbGebunden. Zustand: New. Über den AutorrnrnDr. Manohar A. Potdar, M.Pharm (BITS Pilani), Ph.D. (Production Management) USA, Currently President Technical, Doshi Consultants Pvt. Ltd., Pharmaceutical Plant Design and Validation Consultants, was a professor emeritus .
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 130,75
Anzahl: 1 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. 531 pages. 9.25x6.10x1.22 inches. In Stock.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 132,38
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Taschenbuch. Zustand: Neu. Modern Aspects of Pharmaceutical Quality Assurance | Developing & Proposing Application models, SOPs, practical audit systems for Pharma Industry | Minal Ghante (u. a.) | Taschenbuch | viii | Englisch | 2025 | Springer | EAN 9789819992737 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Buch. Zustand: Neu. Modern Aspects of Pharmaceutical Quality Assurance | Developing & Proposing Application models, SOPs, practical audit systems for Pharma Industry | Minal Ghante (u. a.) | Buch | viii | Englisch | 2024 | Springer | EAN 9789819992706 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Sprache: Englisch
Verlag: Springer Nature Singapore, Springer Nature Singapore, 2025
ISBN 10: 9819992737 ISBN 13: 9789819992737
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering.
Sprache: Englisch
Verlag: Springer Nature Singapore, Springer Nature Singapore Mär 2024, 2024
ISBN 10: 9819992702 ISBN 13: 9789819992706
Anbieter: buchversandmimpf2000, Emtmannsberg, BAYE, Deutschland
Buch. Zustand: Neu. Neuware -The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing SystemSpringer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 532 pp. Englisch.
EUR 140,72
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Über den AutorrnrnDr. Manohar A. Potdar, M.Pharm (BITS Pilani), Ph.D. (Production Management) USA, Currently President Technical, Doshi Consultants Pvt. Ltd., Pharmaceutical Plant Design and Validation Consultants, was a professor emeritus .
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 185,07
Anzahl: 2 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. 531 pages. 9.25x6.10x1.22 inches. In Stock.
Sprache: Englisch
Verlag: Springer, Springer Mär 2024, 2024
ISBN 10: 9819992702 ISBN 13: 9789819992706
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System.
Sprache: Englisch
Verlag: Springer, Springer Mär 2024, 2024
ISBN 10: 9819992702 ISBN 13: 9789819992706
Anbieter: Books-by-Floh, Paderborn, Deutschland
Buch. Zustand: Neu. Neuware -The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System 532 pp. Englisch.