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Re-Engineering Clinical Trials - Best Practices for Streamlining the Development Process pdf

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Description

 							
  
   Re-Engineering Clinical Trials: Best Practices for Streamlining the Development
Process
  
   by Peter Schueler (Editor), Brendan Buckley
(Editor)
  
  # Publisher: Academic Press; 1 edition (January 2, 2015)
 

  # Language: English
  
  # Pages: 360 pages
  
  # Print ISBN: 9780124202467
 

   Description
  
   The
pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the
high costs associated with drug development, there is a vital need to reform this process in order to provide safe and
effective drugs while still securing a profit. Re-Engineering Clinical Trials
evaluates the trends and challenges associated with the current drug development process and presents solutions that
integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on
the need to simplify drug development and offers you well-established methodologies and best practices based on
real-world experiences from expert authors across industry and academia.
  
  Written for all those involved
in clinical research, development and clinical trial design, this book provides a unique and valuable resource for
streamlining the process, containing costs and increasing drug safety and effectiveness.
  
 
•	Highlights the latest paradigm-shifts and innovation advances in clinical research
  
  •	Offers
easy-to-find best practice sections, lists of current literature and resources for further reading and useful solutions
to day-to-day problems in current drug development
  
  •	Discusses important topics such as safety
profiling, data mining, site monitoring, change management, increasing development costs, key performance indicators and
much more 						

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