Re-Engineering Clinical Trials
Best Practices for Streamlining the Development Process
The first book of its kind to offer best practices and solutions toward streamlining the drug development process to contain costs, integrate new technologies and increase efficiency
Peter Schueler (Edited by), Brendan Buckley (Edited by)
9780124202467
Hardback, published 19 December 2014
360 pages
22.9 x 15.2 x 2.5 cm, 0.75 kg
\""...a good overview of problems facing the pharmaceutical industry in the design and conduct of clinical trials, especially within the current regulatory framework. Score: 74 - 3 Stars\"" --Doody's
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]
Re-Engineering Clinical Trials
Best Practices for Streamlining the Development Process
The first book of its kind to offer best practices and solutions toward streamlining the drug development process to contain costs, integrate new technologies and increase efficiency
Peter Schueler (Edited by), Brendan Buckley (Edited by)
9780124202467
Hardback, published 19 December 2014
360 pages
22.9 x 15.2 x 2.5 cm, 0.75 kg
\""...a good overview of problems facing the pharmaceutical industry in the design and conduct of clinical trials, especially within the current regulatory framework. Score: 74 - 3 Stars\"" --Doody's
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]
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