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Description du livre Etat : New. N° de réf. du vendeur ABLIING23Mar3113020264237
Description du livre Etat : New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book. N° de réf. du vendeur ria9783659126550_lsuk
Description du livre PF. Etat : New. N° de réf. du vendeur 6666-IUK-9783659126550
Description du livre Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -New drug discovery and development is a complex, flexible and cost-effective but systematic process that follows a sequence of clinical steps, rules and regulations governed by the experienced regulatory authorities in each country. The rules laid down by the experienced authorities consistently have need of the code of ethics by which every individual involved in clinical research has to stand. Besides these ethical principles, a clinical trial involves multidisciplinary functions which require concepts and approaches, using modern research tools and techniques. In this book, the authors discuss some of key functions in clinical trial management as drug development process, clinical trials design, good clinical practices, roles and responsibilities of clinical trial personnel, regulatory processes/issues and the processes involved in performing excellent monitoring functions for the successful clinical study. This book also facilitates the understanding of the importance of ethics in clinical studies and the evolution of various guidelines, rules and regulations for the management of a clinical trials. 456 pp. Englisch. N° de réf. du vendeur 9783659126550
Description du livre PAP. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. N° de réf. du vendeur L0-9783659126550
Description du livre Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - New drug discovery and development is a complex, flexible and cost-effective but systematic process that follows a sequence of clinical steps, rules and regulations governed by the experienced regulatory authorities in each country. The rules laid down by the experienced authorities consistently have need of the code of ethics by which every individual involved in clinical research has to stand. Besides these ethical principles, a clinical trial involves multidisciplinary functions which require concepts and approaches, using modern research tools and techniques. In this book, the authors discuss some of key functions in clinical trial management as drug development process, clinical trials design, good clinical practices, roles and responsibilities of clinical trial personnel, regulatory processes/issues and the processes involved in performing excellent monitoring functions for the successful clinical study. This book also facilitates the understanding of the importance of ethics in clinical studies and the evolution of various guidelines, rules and regulations for the management of a clinical trials. N° de réf. du vendeur 9783659126550
Description du livre Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Maurya HarikeshMr. Harikesh maurya has obtained his M.Pharm (Pharmacology) in 2007. Since, then he has well experienced & key skills for handling Clinical Trials and worked as a Sr. CRA in Macleods Pharmaceutical ltd. R & D Centre, M. N° de réf. du vendeur 5133289
Description du livre PAP. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. N° de réf. du vendeur L0-9783659126550