Global New Drug Development (Postgraduate Pharmacy Series)

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9781118414880: Global New Drug Development (Postgraduate Pharmacy Series)
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The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market.

This book offers an introduction to the field of drug development with a clear overview of the different processes that lead to a successful new medicine and of the regulatory pathways that are used to launch a new drug that are both safe and efficacious.

“This is the most comprehensive and detailed book on drug development I have ever read and I feel that it is likely to become a staple of drug development courses, such as those taught at Masters Level in my own University.... I think in the light of increasing integration of company and academic approaches to drug development both sides can read this book.. (and, therefore)... this book could not be more timely. “

Professor Mike Coleman, University of Aston., UK ( from his review of the final manuscript)

Biografía del autor:

Jan Rosier holds a PhD in Pharmaceutical Sciences and a PhD in Management. He is Elan Professor of the Business of Biotechnology at UCD Dublin and is Visiting Professor in new drug development at KU Leuven (University of Leuven, Belgium). He was involved in new drug development for 25 years.
Mark Martens holds a PhD in Pharmaceutical Sciences and is a European Registered Toxicologist (ERT). He has more than 40 years of experience in toxicology, risk assessment and nonclinical drug development. He was Vice President of nonclinical development at Tibotec, the virology franchise of Johnson & Johnson, and is currently a consultant in toxicology and preclinical development.
Josse Thomas graduated as Pharmacist, holds a PhD in Medical Sciences and is registered as a Clinical Pharmacologist. He has over 30 years experience in the pharmaceutical industry, mainly in clinical drug development. He is currently Visiting Professor in clinical drug research at KU Leuven and member of the Medical Research Ethics Committee at the university hospitals UZ Leuven.

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Buchbeschreibung John Wiley Sons Inc, United States, 2014. Hardback. Zustand: New. 1. Auflage. Language: English . Brand New Book. The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market. This book offers an introduction to the field of drug development with a clear overview of the different processes that lead to a successful new medicine and of the regulatory pathways that are used to launch a new drug that are both safe and efficacious. This is the most comprehensive and detailed book on drug development I have ever read and I feel that it is likely to become a staple of drug development courses, such as those taught at Masters Level in my own University. I think in the light of increasing integration of company and academic approaches to drug development both sides can read this book. (and, therefore). this book could not be more timely. Professor Mike Coleman, University of Aston., UK ( from his review of the final manuscript). Bestandsnummer des Verkäufers AAH9781118414880

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Buchbeschreibung John Wiley Sons Inc, United States, 2014. Hardback. Zustand: New. 1. Auflage. Language: English . Brand New Book. The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market. This book offers an introduction to the field of drug development with a clear overview of the different processes that lead to a successful new medicine and of the regulatory pathways that are used to launch a new drug that are both safe and efficacious. This is the most comprehensive and detailed book on drug development I have ever read and I feel that it is likely to become a staple of drug development courses, such as those taught at Masters Level in my own University. I think in the light of increasing integration of company and academic approaches to drug development both sides can read this book. (and, therefore). this book could not be more timely. Professor Mike Coleman, University of Aston., UK ( from his review of the final manuscript). Bestandsnummer des Verkäufers AAH9781118414880

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Buchbeschreibung Wiley John & Sons Sep 2014, 2014. Buch. Zustand: Neu. Neuware - The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market. 402 pp. Englisch. Bestandsnummer des Verkäufers 9781118414880

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Buchbeschreibung Wiley John & Sons Sep 2014, 2014. Buch. Zustand: Neu. Neuware - The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market. 402 pp. Englisch. Bestandsnummer des Verkäufers 9781118414880

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