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Nonclinical Study Contracting and Monitoring: A Practical Guide offers a systematic and straightforward handbook for obtaining high quality preclinical Good Laboratory Practice (GLP) studies. This book is full of real-world examples, processes, procedures, useful templates, checklists and sample reports to provide readers with a better understanding of exactly what happens during all stages of a GLP study and the critical aspects of GLP study design and conduct. Designed for both the novice and experienced scientist, this book covers the GLP regulations and how they impact preclinical studies, the differences between GLP, non-GLP and peer-reviewed studies, preclinical GLP study design, laboratory selection, contracts and business ethics, how to obtain test material for the study, animal sourcing and release for study, preparation of a draft report and much more. By illustrating the overall big picture and tying it together with the individual steps, this book is an essential resource to help scientists ensure a high quality GLP study that passes both scientific and regulatory scrutiny.
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"I particularly liked the detailed checklists that are provided throughout the book...this book is an excellent practical guide on how to perform, contract, monitor and report nonclinical studies. It is well presented and easy to read and will be particularly useful for beginning study monitors and toxicologists."--British Toxicology Society, Issue 43, Winter 2013
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Nonclinical Study Contracting and Monitoring: A Practical Guide
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Nonclinical Study Contracting and Monitoring
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Nonclinical Study Contracting and Monitoring: A Practical Guide
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Nonclinical Study Contracting and Monitoring
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ISBN 13: 9780123978295
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Nonclinical Study Contracting and Monitoring: A Practical Guide offers a systematic and straightforward handbook for obtaining high quality preclinical Good Laboratory Practice (GLP) studies. This book is full of real-world examples, processes, procedures, useful templates, checklists and sample reports to provide readers with a better understanding of exactly what happens during all stages of a GLP study and the critical aspects of GLP study design and conduct. Designed for both the novice and experienced scientist, this book covers the GLP regulations and how they impact preclinical studies, the differences between GLP, non-GLP and peer-reviewed studies, preclinical GLP study design, laboratory selection, contracts and business ethics, how to obtain test material for the study, animal sourcing and release for study, preparation of a draft report and much more. By illustrating the overall big picture and tying it together with the individual steps, this book is an essential resource to help scientists ensure a high quality GLP study that passes both scientific and regulatory scrutiny. 262 pp. Englisch. Codice articolo 9780123978295
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Nonclinical Study Contracting and Monitoring: A Practical Guide
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Elsevier Science Publishing Co Inc, 2013
ISBN 10: 0123978297
ISBN 13: 9780123978295
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Nonclinical Study Contracting and Monitoring
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ISBN 10: 0123978297
ISBN 13: 9780123978295
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Kartoniert / Broschiert. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. A handbook for obtaining high quality preclinical Good Laboratory Practice (GLP) studies. It provides readers with a better understanding of exactly what happens during all stages of a GLP study and the critical aspects of GLP study design and conduct. Codice articolo 5891254
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Nonclinical Study Contracting and Monitoring
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Nonclinical Study Contracting and Monitoring : A Practical Guide
Print on DemandDa: AHA-BUCH GmbH, Einbeck, Germania
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Nonclinical Study Contracting and Monitoring: A Practical Guide offers a systematic and straightforward handbook for obtaining high quality preclinical Good Laboratory Practice (GLP) studies. This book is full of real-world examples, processes, procedures, useful templates, checklists and sample reports to provide readers with a better understanding of exactly what happens during all stages of a GLP study and the critical aspects of GLP study design and conduct. Designed for both the novice and experienced scientist, this book covers the GLP regulations and how they impact preclinical studies, the differences between GLP, non-GLP and peer-reviewed studies, preclinical GLP study design, laboratory selection, contracts and business ethics, how to obtain test material for the study, animal sourcing and release for study, preparation of a draft report and much more. By illustrating the overall big picture and tying it together with the individual steps, this book is an essential resource to help scientists ensure a high quality GLP study that passes both scientific and regulatory scrutiny. Codice articolo 9780123978295
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