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Interface between Regulation and Statistics in Drug Development (Hardcover)
Loot Price: R3,451
Discovery Miles 34 510
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Interface between Regulation and Statistics in Drug Development (Hardcover)
Series: Chapman & Hall/CRC Biostatistics Series
Expected to ship within 12 - 17 working days
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With the critical role of statistics in the design, conduct,
analysis and reporting of clinical trials or observational studies
intended for regulatory purposes, numerous guidelines have been
issued by regulatory authorities around the world focusing on
statistical issues related to drug development. However, the
available literature on this important topic is sporadic, and often
not readily accessible to drug developers or regulatory personnel.
This book provides a systematic exposition of the interplay between
the two disciplines, including emerging themes pertaining to the
acceleration of the development of pharmaceutical medicines to
serve patients with unmet needs. Features: Regulatory and
statistical interactions throughout the drug development continuum
The critical role of the statistician in relation to the changing
regulatory and healthcare landscapes Statistical issues that
commonly arise in the course of drug development and regulatory
interactions Trending topics in drug development, with emphasis on
current regulatory thinking and the associated challenges and
opportunities The book is designed to be accessible to readers with
an intermediate knowledge of statistics, and can be a useful
resource to statisticians, medical researchers, and regulatory
personnel in drug development, as well as graduate students in the
health sciences. The authors' decades of experience in the
pharmaceutical industry and academia, and extensive regulatory
experience, comes through in the many examples throughout the book.
General
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