Pharmaceutical Science & Regulation

PUBLISHED


Viewing: 1 - 4 of 4
Published:
December 15, 2013
Author(s):
Urmila Diwekar
The book describes various unit operations in batch and bioprocessing and design methods for these units. Numerical methods are necessary to solve these design problems. The time-dependent nature of batch processes result in challenging scheduling and planning problems. Further, every unit 
  Hardback
$149.95
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Published:
January 15, 2014
Author(s):
Sarfaraz K. Niazi
This comprehensive bioprocessing textbook deals with the fundamentals, basic concepts, definitions, methods, and applications of the use of biological catalysts to produce products of high value and utility, from alcohol to recombinant monoclonal antibodies to common day use fuel. It covers all 
  Hardback
$129.95
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Published:
March 15, 2014
Author(s):
Scott Evans; Naitee Ting
With complete coverage of issues in all phases of clinical trials, including design, data monitoring, analyses, interpretation, and reporting, this book provides an overview of fundamental concepts important to statisticians working with clinical trials. It examines issues related to product 
  Hardback
$79.95
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Published:
March 15, 2014
Author(s):
Maria A. Hernandez, Ph.D.; Appu Rathinavelu, Ph.D.

  Hardback
$87.95
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NEW for 2010!

Bayesian Adaptive Methods for Clinical Trials
"This fine book represents the most recent and exciting developments in this area, and gives ample justification for the power and elegance of Bayesian trial design and analysis. ... a major contribution to the science and practice of clinical trials."
-David J. Spiegelhalter, MRC Biostatistics Unit, University of Cambridge, UK
Also available in eBook!

Find more help with designing clinical trials

 


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Journal of Biopharmaceutical Statistics

 


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