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Interface between Regulation and Statistics in Drug Development
Af: Birol Emir, Michael Gaffney, Demissie Alemayehu
Engelsk
Bogcover for Interface between Regulation and Statistics in Drug Development af Birol Emir, Michael Gaffney, Demissie Alemayehu, 9780367608286
Specifikationer
Sprog:
Engelsk
Sider:
146
ISBN-13:
9780367608286
Indbinding:
Paperback
ISBN-10:
0367608286
Kategori:
Udg. Dato:
1 aug 2022
Størrelse i cm:
15,5 x 23,4 x 1,6
Forlag:
Serie:
Oplagsdato:
1 aug 2022
Forfatter(e):
Genre:

Interface between Regulation and Statistics in Drug Development

Af: Birol Emir, Michael Gaffney, Demissie Alemayehu
Engelsk
Paperback 2022
Format:
Paperback
Bog beskrivelse

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.

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    Specifikationer
    Sprog:
    Engelsk
    Sider:
    146
    ISBN-13:
    9780367608286
    Indbinding:
    Paperback
    ISBN-10:
    0367608286
    Kategori:
    Udg. Dato:
    1 aug 2022
    Størrelse i cm:
    15,5 x 23,4 x 1,6
    Forlag:
    Serie:
    Oplagsdato:
    1 aug 2022
    Forfatter(e):
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