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The Drug Development Process: Increasing Efficiency and Cost-Effectiveness(Drugs and the Pharmaceutical Sciences)

The Drug Development Process: Increasing Efficiency and Cost-Effectiveness(Drugs and the Pharmaceutical Sciences)


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About the Book

Examines the entire pharmaceutical development process, emphasizing approaches to increasing efficiency and reducing costs. Challenges current avenues of drug development used by industry and regulatory agencies and presents alternatives that seek to improve outdated processes.

Table of Contents:
Changing Perspectives in Drug Development The Evolving Drug Discovery and Development Process, John C. Somberg Redefining Competition in the Pharmaceutical Industry: A Time for Choice, John Thompson and Jan Gugliotti Process Challenges in Drug Development The Impact of Liability and Cost Containment on the Drug Development Process, Martha M. Rumore Managing the Overall Portfolio for Successful Discover and Development, Rebecca J. Anderson Pharmaceutical and Formulation Factors Pharmaceutical Issues in Drug Development, Umesh V. Banakar and Michael C. Makoid Novel Drug Delivery Systems, Bret Berner and Agis Kydonieus Drug Design, Pharmacokinetics, and Toxicology Computer-Aided Drug Design, Terry R. Stouch New Approaches to Nonclinical Biodisposition Studies, D. Bruce Campbell Changes in Pharmacokinetics and Drug Metabolism Responsability in Drug Discovery and Development, Peter G. Welling Chemotherapy Anticancer Drug Development, Jim Cassidy Clinical Studies and the Use of Clinical Research Organizations Clinical Pharmacology in Drug Development: A View to Future Effectiveness, J. Robert Powell, Alan Bye, and Paul D. Rubin Contracting CROs in Your Organization: New Strategies for New Challenges, Gary D. Lightfoot and John R. Vogel The Role of Clinical Research Organizations in Drug Development, Albert J. Siemens and James E. Higgins European and Japanese Approaches Understanding Drug Development and Registration in Japan, W. J. C. Currie Increasing the Effectiveness of Clinical Pathology Testing and its Value to Drug Development in Europe, Dai Davies and Karolyn Jackson New Marketing Authorization Procedures in the European Union and the Impact on Regulatory Strategy, Vaila M. Marshall

Review :
"Presentations considering legal issues and their relationship to cost effectiveness, opportunities for optimal use of contract research reorganization, and foreign drug development achievements are highlights of the book. "-Journal of Medicinal Chemistry From the Foreword" The authorsin this book have thought and written about a variety of subjects that need to be considered in re-engineering, the drug development process to meet the challenges of the future. This book gives the readers the opportunity to think with these experts as they address specific problems faced by readers in trying to increase the efficiency and effectiveness of their part of the drug development process. "-Marcus M. Reidenberg. M.D., Departments of Pharmacology and Medicine, Cornell University Medical College, NY, NY


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Product Details
  • ISBN-13: 9780824797270
  • Publisher: Taylor & Francis Inc
  • Publisher Imprint: Marcel Dekker Inc
  • Height: 229 mm
  • No of Pages: 472
  • Returnable: N
  • Sub Title: Increasing Efficiency and Cost-Effectiveness
  • Width: 152 mm
  • ISBN-10: 0824797272
  • Publisher Date: 15 Aug 1996
  • Binding: Hardback
  • Language: English
  • No of Pages: 472
  • Series Title: Drugs and the Pharmaceutical Sciences
  • Weight: 771 gr


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The Drug Development Process: Increasing Efficiency and Cost-Effectiveness(Drugs and the Pharmaceutical Sciences)
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