EUR 8,18
Anzahl: 1 verfügbar
In den WarenkorbZustand: New.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 6,10
Anzahl: 1 verfügbar
In den WarenkorbPaperback. Zustand: Brand New. 106 pages. 8.00x5.00x0.24 inches. In Stock.
Anbieter: Ammareal, Morangis, Frankreich
Softcover. Zustand: Très bon. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Ammareal gives back up to 15% of this item's net price to charity organizations.
Sprache: Englisch
ISBN 10: 935290320X ISBN 13: 9789352903207
Anbieter: Majestic Books, Hounslow, Vereinigtes Königreich
EUR 7,35
Anzahl: 4 verfügbar
In den WarenkorbZustand: New. pp. 224.
Anbieter: Majestic Books, Hounslow, Vereinigtes Königreich
EUR 8,64
Anzahl: 1 verfügbar
In den WarenkorbZustand: New. pp. 262.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 17,30
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
EUR 16,95
Anzahl: 4 verfügbar
In den WarenkorbZustand: New. pp. 328.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 21,54
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 23,71
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 26,75
Anzahl: 2 verfügbar
In den WarenkorbPaperback. Zustand: Brand New. 218 pages. 5.50x0.46x8.50 inches. In Stock.
Sprache: Englisch
Verlag: PharmaMed Press / BSP Books, 2021
ISBN 10: 9390211522 ISBN 13: 9789390211524
Anbieter: Vedams eBooks (P) Ltd, New Delhi, Indien
Hardcover. Zustand: New. This handbook is fully updated to the current regulatory requirement in the pharmaceutical laboratory world. Purpose of book is to assist individual on Gx Prequirement, good manufacturing practices, good laboratory practices, performance monitoring and root cause analysis and quality triangles The purpose of this hand book is to provide easily accessible knowledge about the good laboratory practices. In current pharmaceutical world we need a fast and reliable source of techniques to implement the system and resolve problem. This handbook gives pathway for us to take right decision. Nothing comes in one box for us. Changes happen with or without us. The higher we go in the organization, the more complex ore challenges become .This book gives overall view of quality laboratory system. We hope this handbook can contributes to assemble lots of related materials and package them in one place for easy reference and access. I encourage you to read, enjoy, study and learn from this book and go forth and empower you/ your teams to lead you and your organization to world class results. Contents: 1. Overview of Good Laboratory Practices in Pharmaceutical Industry 2. Overview of Good Microbiology Practices in Pharmaceutical Industry 3. Quality Assurance Management in GLP Environment 4. Laboratory Quality Manual 5. Laboratory Quality Policy 6. Laboratory Site Master Files 7. Validation Master Plan 8. Laboratory Computer-Software Validation and Qualification 9. Control of Spreadsheets in GLP 10. Analytical Instrument and Equipment Qualification 11. Electronic and Paper-Based Data Management in GLP 12. Laboratory Training and Qualification Management Program 13. Reviewer Qualification Management 14. Label Management in GLP Environment 15. Glassware Management in GLP 16. GLP Column Management 17. GLP Standard Operating Procedure (SOP) Management 18. GLP Specification Management 19. GLP Certificate o.
Sprache: Mittelenglisch
Verlag: B.R. Publishing Corporation, 2018
ISBN 10: 9386223872 ISBN 13: 9789386223876
Anbieter: Majestic Books, Hounslow, Vereinigtes Königreich
EUR 17,41
Anzahl: 4 verfügbar
In den WarenkorbZustand: New.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 34,36
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Sprache: Deutsch
ISBN 10: 3945191777 ISBN 13: 9783945191774
Anbieter: medimops, Berlin, Deutschland
Zustand: good. Befriedigend/Good: Durchschnittlich erhaltenes Buch bzw. Schutzumschlag mit Gebrauchsspuren, aber vollständigen Seiten. / Describes the average WORN book or dust jacket that has all the pages present.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 42,88
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Verlag: PharmaMed Press/BSP Books, 2019
Anbieter: Vedams eBooks (P) Ltd, New Delhi, Indien
Soft cover. Zustand: New. Contents: 1. GMP Regulations for Pharmaceutical Industry. 2. Good Laboratory Practices in Pharmaceutical Industry. 3. Good Microbiology Practice in Pharmaceutical Industry. 4. Good Aseptic Practices in Pharmaceutical Industry. 5. Good Clean Room Monitoring in Pharmaceutical Industry. 6. Good Engineering Practices in Pharmaceutical Industry. 7. Good Alarm Management Practices in Pharmaceutical Industry. 8. Good Computer Validation System Practices in Pharmaceutical Industry. 9. Good Distribution Practices Supply Chain Integrity in Pharmaceutical Industry. 10. Good Data Management System in Pharmaceutical Industry. 11. Quality Agreements in Pharmaceutical Industry. 12. Change control Management and its Applications. 13. Technology Transfer of Pharmaceutical Product. 14. Pharmaceutical Annual Product Quality Review. 15. Statistical Tools for Pharmaceutical Industry. 16. Application of Different Quality Tools in Investigation of Non-Conformance Observations. 17. New Approach to the Internal Audit from Traditional to Risk based Approach. 18. Quality by Design (QbD) Approach in the Product Life Cycle. 19. Process Validation in Pharmaceutical Industry. 20. Cleaning Validation and Cross Contamination Approach on Risk MaPP Concept. 21. Pharmaceutical Water Generation and Distribution System and Regulatory Expectation. 22. Pharmaceutical Heating, Ventilation and Air Conditionings (HVAC) and Regulatory Expectations. 23. Manufacturing Execution System (MES) in Pharmaceutical Industry. 24. Pharmaceutical Drug Master File. 25. Common Technical Document in Regulatory Filing. 26. European Union Marketing Authorization. 27. Site Master File. 28. Standard Operating Procedure (SOP). 29. Quality Manual. 30. Human Error Reduction: Pharma Industry Challenge. 31. Regulatory Inspections: Face Challenges through Proactive Measures. 32. Pharmaceutical GMP: Past, Present, and Future A Review. This handbook has been written for the students of pharmacy and pharmaceutical industry. It gives pocket guide of good manufacturing practices in pharmaceutical industry. The purpose of this handbook is to provide easily accessible knowledge about the pharmaceutical industry and to assist individuals to know about pharmaceutical world. This handbook has also incorporated the current trends and expectations of the evolving pharmaceutical industry and regulatory oversight. In current pharmaceutical world we need a fast and reliable source of techniques to implement the system and resolve problem. This handbook gives pathway for us to take right decision. Nothing comes in a one box for us. Changes happen with or without us. The higher we go in the organization, the more complex our challenges become. This book gives overall view of quality management system. (jacket).
EUR 22,08
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Über den AutorAVADHOOT DONGARE started writing fiction in 2007. He has published four novels in Marathi: Svatahala Faltu Samjanyachi Goshta (The Story of Being Useless, 2012), Eka Lekhakache Teen Sandarbha (Three Contexts of a Write.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 60,37
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: Neu. Neuware - Avadhoot Dongare is a young promising Marathi novelist. He was awarded the Sahitya Akademi Yuva Puraskar, 2014, for Svatahala Faltu Samjanyachi Goshta (The Story of Being Useless). He has a phenomenally different way of telling a story. Once he starts telling the story, he moves out of the picture. The characters start behaving independently.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 75,00
Anzahl: 2 verfügbar
In den WarenkorbPaperback. Zustand: Brand New. 77 pages. 9.25x6.10x0.28 inches. In Stock.
EUR 80,24
Anzahl: 1 verfügbar
In den WarenkorbHRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 74,03
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Taschenbuch. Zustand: Neu. Neuware - Translation of: Påana, påaònåi ni pravåaha.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 87,72
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Sprache: Englisch
Verlag: LAP LAMBERT Academic Publishing, 2022
ISBN 10: 6205510308 ISBN 13: 9786205510308
Anbieter: moluna, Greven, Deutschland
EUR 53,35
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New.
Anbieter: Kennys Bookstore, Olney, MD, USA
Zustand: New. 2019. Illustrated. Hardcover. . . . . . Books ship from the US and Ireland.
Sprache: Englisch
Verlag: LAP LAMBERT Academic Publishing, 2022
ISBN 10: 6205510308 ISBN 13: 9786205510308
Anbieter: preigu, Osnabrück, Deutschland
Taschenbuch. Zustand: Neu. DFT BASED STUDY OF BIOLOGICALLY ACTIVE HETEROCYCLIC COMPOUNDS | Rameshwar Dongare (u. a.) | Taschenbuch | Englisch | 2022 | LAP LAMBERT Academic Publishing | EAN 9786205510308 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
Zustand: New. Über den AutorrnrnTrupti Patil-Dongare has over 14 years of experience in pharmaceutical industry in quality assurance, quality Control, regulatory compliance and production. I am Master in Industrial Pharmacy from Osmania University, Hyder.
EUR 93,60
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Über den AutorrnrnTrupti Patil-Dongare has over 16 years of experience in pharmaceutical industry. Trupti has completed Doctor of Philosophy in Pharmacy, Master s in industrial pharmacy, Advance Diploma in Quality Assurance and IRCA approve.