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Clinical Trials Risk Management
Contributor(s): Robinson, Martin (Author), Cook, Simon (Author)
ISBN: 0849333237     ISBN-13: 9780849333231
Publisher: CRC Press
OUR PRICE:   $209.00  
Product Type: Hardcover - Other Formats
Published: October 2005
Qty:
Annotation: Drug development is risky business. It is against the backdrop of huge financial, scientific, technical and medical risks that a clinical trials manager is expected to function, effectively identifying and managing all project risks, to deliver a successful outcome. Focusing on the day-to-day needs of a clinical trials manager, Clinical Trials Risk Management explains the key concepts and principles of risk management, as well as showing how best to how to apply them directly to 'real life' clinical trial situations. After building a foundation of basic principles, the authors lead you through specific methods for handling the risks characteristically encountered in clinical trials. Their combined years of experience in pharmaceutical research and development shine through the narrative, making the prose both lively and informative. They discuss concepts using worked examples and include a summary of the main points at the end of each chapter. In addition to diagrams and Risk and Precision Tree charts, the text is sprinkled with humorous line drawings that reinforce the concepts. After reading this book, you will know how to: ??Prepare a Risk Assessment ??Design an Impact-Probability Matrix ??Compile a Risk Register ??Run a Monte Carlo Simulation ??Set up a Project Decision Tree ??Plan preventative and contingency actions The stand-alone chapters provide easy access to topics, while anecdotal and visual examples make them easy to remember. Martin Robinson and Simon Cook deliver a clear interpretation of complex information, thus saving you the time it would take to wade through a lengthier text, adopting a straightforward approach to examining clinical trials from a risk manager'sperspective. A practical, readable guide, the book is filled with information that can be put to immediate use to improve current or planned clinical trials.
Additional Information
BISAC Categories:
- Medical | Pharmacy
- Medical | Pharmacology
Dewey: 615.19
LCCN: 2005051479
Physical Information: 0.7" H x 6.46" W x 9.52" (1.02 lbs) 232 pages
 
Descriptions, Reviews, Etc.
Publisher Description:

Drug development is risky business. It is against the backdrop of huge financial, scientific, technical and medical risks that a clinical trials manager is expected to function, effectively identifying and managing all project risks, to deliver a successful outcome. Focusing on the day-to-day needs of a clinical trials manager, Clinical Trials Risk Management explains the key concepts and principles of risk management, as well as showing how best to how to apply them directly to 'real life' clinical trial situations.

After building a foundation of basic principles, the authors lead you through specific methods for handling the risks characteristically encountered in clinical trials. Their combined years of experience in pharmaceutical research and development shine through the narrative, making the prose both lively and informative. They discuss concepts using worked examples and include a summary of the main points at the end of each chapter. In addition to diagrams and Risk and Precision Tree charts, the text is sprinkled with humorous line drawings that reinforce the concepts.

After reading this book, you will know how to:

  • Prepare a Risk Assessment
  • Design an Impact-Probability Matrix
  • Compile a Risk Register
  • Run a Monte Carlo Simulation
  • Set up a Project Decision Tree
  • Plan preventative and contingency actions

    The stand-alone chapters provide easy access to topics, while anecdotal and visual examples make them easy to remember. Martin Robinson and Simon Cook deliver a clear interpretation of complex information, thus saving you the time it would take to wade through a lengthier text, adopting a straightforward approach to examining clinical trials from a risk manager's perspective. A practical, readable guide, the book is filled with information that can be put to immediate use to improve current or planned clinical trials.