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Intelligent Drug Development - Trials and Errors in Clinical Research (Hardcover)
Loot Price: R1,798
Discovery Miles 17 980
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Intelligent Drug Development - Trials and Errors in Clinical Research (Hardcover)
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Clinical research is heavily regulated and involves coordination of
numerous pharmaceutical-related disciplines. Each individual trial
involves contractual, regulatory, and ethics approval at each site
and in each country. Clinical trials have become so complex and
government requirements so stringent that researchers often
approach trials too cautiously, convinced that the process is bound
to be insurmountably complicated and riddled with roadblocks. A
step back is needed, an objective examination of the drug
development process as a whole, and recommendations made for
streamlining the process at all stages. With Intelligent Drug
Development, Michael Tansey systematically addresses the key
elements that affect the quality, timeliness, and
cost-effectiveness of the drug-development process, and identifies
steps that can be adjusted and made more efficient. Tansey uses his
own experiences conducting clinical trials to create a guide that
provides flexible, adaptable ways of implementing the necessary
processes of development. Moreover, the processes described in the
book are not dependent either on a particular company structure or
on any specific technology; thus, Tansey's approach can be
implemented at any company, regardless of size. The book includes
specific examples that illustrate some of the ways in which the
principles can be applied, as well as suggestions for providing a
better context in which the changes can be implemented. The
protocols for drug development and clinical research have grown
increasingly complex in recent years, making Intelligent Drug
Development a needed examination of the pharmaceutical process.
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