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Aggiungi al carrelloHRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.
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Da: BennettBooksLtd, San Diego, NV, U.S.A.
hardcover. Condizione: New. In shrink wrap. Looks like an interesting title!
Da: Books Puddle, New York, NY, U.S.A.
Condizione: New. pp. 232.
Da: Chiron Media, Wallingford, Regno Unito
EUR 225,19
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Aggiungi al carrelloHardcover. Condizione: New.
Da: GreatBookPrices, Columbia, MD, U.S.A.
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Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 227,39
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Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irlanda
EUR 262,70
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Aggiungi al carrelloCondizione: New. A Practical Guide to Quality Management in Clinical Trial Research Num Pages: 232 pages, 5 black & white illustrations, 14 black & white tables. BIC Classification: KJMQ; KNDP. Category: (P) Professional & Vocational. Dimension: 235 x 156 x 18. Weight in Grams: 477. . 2005. Hardback. . . . .
Da: Revaluation Books, Exeter, Regno Unito
EUR 278,18
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Aggiungi al carrelloHardcover. Condizione: Brand New. 1st edition. 214 pages. 9.25x6.25x0.75 inches. In Stock.
EUR 246,92
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Aggiungi al carrelloCondizione: New. Graham OggSetting up a GXP environment where none existed previously is a very daunting task. Getting staff to write down what they do for every task is a correspondingly difficult and time-consuming exercise. Examining how to maintain quality contro.
Editore: Taylor and Francis Inc, US, 2005
ISBN 10: 0849397227 ISBN 13: 9780849397226
Lingua: Inglese
Da: Rarewaves.com USA, London, LONDO, Regno Unito
EUR 323,61
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Aggiungi al carrelloHardback. Condizione: New. Setting up a GXP environment where none existed previously is a very daunting task. Getting staff to write down what they do for every task is a correspondingly difficult and time-consuming exercise. Examining how to maintain quality control in clinical trial research, A Practical Guide to Quality Management in Clinical Trial Research provides a cornerstone of knowledge for establishing a quality system that complies with the relevant regulations. There are many books available that cover how to interpret regulations. Going a step or two further, this book provides practical advice that is useful on a daily basis.The book contains information for various standards including GLPs, GCPs, and GMPs. It gives detailed explanations of how to prepare, update, and maintain SOPs and includes advice on training and development of personnel. Drawing directly on his years of experience, the author delineates a from-the-trenches methodology that creates a value-added quality management system from a business perspective. He provides a solid foundation as well as tips and techniques for establishing a quality system that will comply with all the relevant regulations. The author's integrated approach and anecdotal style turns technically accurate information into easy reading. The book arms you with tools and concepts that you can use to go beyond regulatory compliance and move into the realm of business quality improvement.
Da: Kennys Bookstore, Olney, MD, U.S.A.
Condizione: New. A Practical Guide to Quality Management in Clinical Trial Research Num Pages: 232 pages, 5 black & white illustrations, 14 black & white tables. BIC Classification: KJMQ; KNDP. Category: (P) Professional & Vocational. Dimension: 235 x 156 x 18. Weight in Grams: 477. . 2005. Hardback. . . . . Books ship from the US and Ireland.
EUR 272,10
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Aggiungi al carrelloBuch. Condizione: Neu. A Practical Guide to Quality Management in Clinical Trial Research | Graham Ogg | Buch | Einband - fest (Hardcover) | Englisch | 2005 | CRC Press | EAN 9780849397226 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu.
Da: Revaluation Books, Exeter, Regno Unito
EUR 342,53
Quantità: 2 disponibili
Aggiungi al carrelloHardcover. Condizione: Brand New. 1st edition. 214 pages. 9.25x6.25x0.75 inches. In Stock.
Editore: Taylor and Francis Inc, US, 2005
ISBN 10: 0849397227 ISBN 13: 9780849397226
Lingua: Inglese
Da: Rarewaves.com UK, London, Regno Unito
EUR 293,27
Quantità: 1 disponibili
Aggiungi al carrelloHardback. Condizione: New. Setting up a GXP environment where none existed previously is a very daunting task. Getting staff to write down what they do for every task is a correspondingly difficult and time-consuming exercise. Examining how to maintain quality control in clinical trial research, A Practical Guide to Quality Management in Clinical Trial Research provides a cornerstone of knowledge for establishing a quality system that complies with the relevant regulations. There are many books available that cover how to interpret regulations. Going a step or two further, this book provides practical advice that is useful on a daily basis.The book contains information for various standards including GLPs, GCPs, and GMPs. It gives detailed explanations of how to prepare, update, and maintain SOPs and includes advice on training and development of personnel. Drawing directly on his years of experience, the author delineates a from-the-trenches methodology that creates a value-added quality management system from a business perspective. He provides a solid foundation as well as tips and techniques for establishing a quality system that will comply with all the relevant regulations. The author's integrated approach and anecdotal style turns technically accurate information into easy reading. The book arms you with tools and concepts that you can use to go beyond regulatory compliance and move into the realm of business quality improvement.
Da: Majestic Books, Hounslow, Regno Unito
EUR 247,19
Quantità: 3 disponibili
Aggiungi al carrelloCondizione: New. pp. 232 Illus. This item is printed on demand.
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 248,94
Quantità: 4 disponibili
Aggiungi al carrelloCondizione: New. PRINT ON DEMAND pp. 232.
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 256,41
Quantità: 1 disponibili
Aggiungi al carrelloBuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Examining how to maintain assured quality in clinical trial research, A Practical Guide to Quality Management in Clinical Trial Research provides solid foundations, tips, and techniques for establishing a quality system that will comply with the relevant regulations. This book offers useful information for various standards including Good Laboratory Practice, Good Clinical Practice, and Good Manufacturing Practice. It gives detailed explanations of how to prepare, update, and maintain Standard Operating Procedures and also includes advice on training and development of personnel. This text is ideal for clinical trial monitors and quality assurance personnel in the pharmaceutical industry.