Sprache: Englisch
Verlag: Wiley-Interscience, U.S.A., 2006
ISBN 10: 0471738409 ISBN 13: 9780471738404
Anbieter: The Book Exchange, Macclesfield, CHESH, Vereinigtes Königreich
EUR 9,11
Anzahl: 1 verfügbar
In den WarenkorbHardcover. Zustand: Near Fine. 0471738409. Includes UNUSED, sealed CD-ROM. A near fine unread Pictorial board hardcover, from closed pharmaceutical company library. Lending record shows this book has never been borrowed. Index, illustrated with tables. Pharmaceutical laboratories must demonstrate sustainable operational practices that ensure compliance with the current good manufacturing practice (CGMP) regulations. This book provides laboratory supervisors with an audit system that they can rely on to ensure their facility remains compliant. Paper clip mark on front endpapers, otherwise contents as new, clean, tight and bright. Book.
Sprache: Englisch
Verlag: Wiley-Interscience, U.S.A., 2006
ISBN 10: 0471738409 ISBN 13: 9780471738404
Anbieter: The Book Exchange, Macclesfield, CHESH, Vereinigtes Königreich
EUR 28,59
Anzahl: 1 verfügbar
In den WarenkorbHardcover. Zustand: Near Fine. 0471738409. Includes UNUSED, sealed CD-ROM. A near fine unread Pictorial board hardcover, from closed pharmaceutical company library. Lending record shows this book has never been borrowed. Index, illustrated with tables. Pharmaceutical laboratories must demonstrate sustainable operational practices that ensure compliance with the current good manufacturing practice (CGMP) regulations. This book provides laboratory supervisors with an audit system that they can rely on to ensure their facility remains compliant. Paper clip mark on front endpapers, otherwise contents as new, clean, tight and bright. Book.
Zustand: Good. Exact ISBN match. Immediate shipping. No funny business.
Anbieter: PBShop.store UK, Fairford, GLOS, Vereinigtes Königreich
EUR 112,06
Anzahl: 15 verfügbar
In den WarenkorbUNK. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Anbieter: Brook Bookstore On Demand, Napoli, NA, Italien
EUR 111,36
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In den WarenkorbZustand: new.
Anbieter: BennettBooksLtd, Los Angeles, CA, USA
hardcover. Zustand: New. In shrink wrap. Looks like an interesting title!
Sprache: Englisch
Verlag: Wiley (2020), (Hoboken, N. J.), 2020
ISBN 10: 1119529239 ISBN 13: 9781119529231
Zustand: NF. Hardcover book bound in glazed pictorial boards. 24 cm. 302 pages. The book is in near fine condition. No ownership marks/writing present within. Hinges tight, interior pages bright. Light bumping to the covers.
Anbieter: Brook Bookstore On Demand, Napoli, NA, Italien
EUR 130,39
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: new.
Anbieter: GreatBookPrices, Columbia, MD, USA
EUR 140,95
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: As New. Unread book in perfect condition.
Anbieter: GreatBookPrices, Columbia, MD, USA
EUR 143,18
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In den WarenkorbZustand: New.
Anbieter: THE SAINT BOOKSTORE, Southport, Vereinigtes Königreich
EUR 131,43
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In den WarenkorbHardback. Zustand: New. New copy - Usually dispatched within 4 working days.
EUR 145,06
Anzahl: 3 verfügbar
In den WarenkorbZustand: New. pp. viii + 291 Illus.
Anbieter: PBShop.store UK, Fairford, GLOS, Vereinigtes Königreich
EUR 147,63
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In den WarenkorbHRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Anbieter: GreatBookPricesUK, Woodford Green, Vereinigtes Königreich
EUR 142,69
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In den WarenkorbZustand: As New. Unread book in perfect condition.
Anbieter: GreatBookPricesUK, Woodford Green, Vereinigtes Königreich
EUR 141,73
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In den WarenkorbZustand: New.
Anbieter: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irland
EUR 148,99
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In den WarenkorbZustand: New. Validating Chromatographic Methods: A Practical Guide intends to bring order to the potentially chaotic process of methods validation. It provides the novice with enough practical information and tools to keep from having to reinvent the wheel by having to develop their own systems to attach methods validation from scratch. Num Pages: 304 pages, Illustrations. BIC Classification: PNFC. Category: (P) Professional & Vocational. Dimension: 241 x 164 x 21. Weight in Grams: 596. . 2006. Hardcover. . . . .
Zustand: New. pp. viii + 291.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 156,95
Anzahl: 2 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. hardback/cd-rom edition. 291 pages. 9.50x6.25x0.75 inches. In Stock.
Anbieter: THE SAINT BOOKSTORE, Southport, Vereinigtes Königreich
EUR 154,04
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In den WarenkorbHardback. Zustand: New. New copy - Usually dispatched within 4 working days.
Anbieter: Majestic Books, Hounslow, Vereinigtes Königreich
EUR 170,80
Anzahl: 3 verfügbar
In den WarenkorbZustand: New.
Anbieter: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irland
Erstausgabe
EUR 174,98
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In den WarenkorbZustand: New. 2020. 1st Edition. Hardcover. . . . . .
Zustand: New.
EUR 186,45
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. Validating Chromatographic Methods: A Practical Guide intends to bring order to the potentially chaotic process of methods validation. It provides the novice with enough practical information and tools to keep from having to reinvent the wheel by having to develop their own systems to attach methods validation from scratch. Num Pages: 304 pages, Illustrations. BIC Classification: PNFC. Category: (P) Professional & Vocational. Dimension: 241 x 164 x 21. Weight in Grams: 596. . 2006. Hardcover. . . . . Books ship from the US and Ireland.
EUR 141,74
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. DAVID M. BLIESNER, PhD, is the founder and President of Delphi Analytical Services, Inc., in Indian Rocks Beach, Florida, a company offering training, training technology, and compliance products and services to the pharmaceutical, biopharmaceutical, medica.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 185,14
Anzahl: 2 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. hardback/cd-rom edition. 277 pages. 9.25x6.25x0.75 inches. In Stock.
EUR 149,47
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. DAVID M. BLIESNER, Ph.D., is Founder and President of Delphi Analytical Services, Inc. He provides CGMP consulting and training services to the pharmaceutical, biopharmaceutical, contract analytical laboratory, and allied industries. He possesses a unique c.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 199,92
Anzahl: 2 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. 302 pages. 9.00x6.25x1.00 inches. In Stock.
Anbieter: Kennys Bookstore, Olney, MD, USA
EUR 218,58
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In den WarenkorbZustand: New. 2020. 1st Edition. Hardcover. . . . . . Books ship from the US and Ireland.
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - Develop an understanding of FDA and global regulatory agency requirements for Laboratory Control System (LCS) operationsIn Laboratory Control System Operations in a GMP Environment, readers are given the guidance they need to implement a CGMP compliant Laboratory Control System (LCS) that fits within Global Regulatory guidelines. Using the Quality Systems Approach, regulatory agencies like the FDA and the European Medicine Agency have developed a scheme of systems for auditing pharmaceutical manufacturing facilities which includes evaluating the LCS. In this guide, readers learn the fundamental rules for operating a CGMP compliant Laboratory Control System.Designed to help leaders meet regulatory standards and operate more efficiently, the text includes chapters that cover Laboratory Equipment Qualification and Calibration, Laboratory Facilities, Method Validation and Method Transfer, Laboratory Computer Systems, Laboratory Investigations as well as Data Governance and Data Integrity. The text also includes chapters related to Laboratory Managerial and Administrative Systems, Laboratory Documentation Practices and Standard Operating Procedures and General Laboratory Compliance Practices. Additionally, a chapter outlining Stability Program operations is included in the text.In addition to these topics, it includes LCS information and tools such as:\* End of chapter templates, checklists, and LCS guidance to help you follow the required standards\* Electronic versions of each tool so users can use them outside of the text\* An In-depth understanding of what is required by the FDA and other globally significant regulatory authorities for GMP compliant systemsFor quality assurance professionals working within the pharmaceutical or biopharma industries, this text provides the insight and tools necessary to implement government-defined regulations.
Sprache: Englisch
Verlag: John Wiley & Sons Inc, New York, 2020
ISBN 10: 1119529239 ISBN 13: 9781119529231
Anbieter: Grand Eagle Retail, Bensenville, IL, USA
Hardcover. Zustand: new. Hardcover. Develop an understanding of FDA and global regulatory agency requirements for Laboratory Control System (LCS) operations In Laboratory Control System Operations in a GMP Environment, readers are given the guidance they need to implement a CGMP compliant Laboratory Control System (LCS) that fits within Global Regulatory guidelines. Using the Quality Systems Approach, regulatory agencies like the FDA and the European Medicine Agency have developed a scheme of systems for auditing pharmaceutical manufacturing facilities which includes evaluating the LCS. In this guide, readers learn the fundamental rules for operating a CGMP compliant Laboratory Control System. Designed to help leaders meet regulatory standards and operate more efficiently, the text includes chapters that cover Laboratory Equipment Qualification and Calibration, Laboratory Facilities, Method Validation and Method Transfer, Laboratory Computer Systems, Laboratory Investigations as well as Data Governance and Data Integrity. The text also includes chapters related to Laboratory Managerial and Administrative Systems, Laboratory Documentation Practices and Standard Operating Procedures and General Laboratory Compliance Practices. Additionally, a chapter outlining Stability Program operations is included in the text. In addition to these topics, it includes LCS information and tools such as: End of chapter templates, checklists, and LCS guidance to help you follow the required standards Electronic versions of each tool so users can use them outside of the text An In-depth understanding of what is required by the FDA and other globally significant regulatory authorities for GMP compliant systems For quality assurance professionals working within the pharmaceutical or biopharma industries, this text provides the insight and tools necessary to implement government-defined regulations. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.