Buy Designing Science Presentations: A Visual Guide to Figures, Papers, Slides, Posters, and More 2nd Edition PDF ebook by author Matt Carter – published by Academic Press in 2021 and save up to 80% compared to the print version of this textbook. With PDF version of this textbook, not only save you money, you can also highlight, add text, underline add post-it notes, bookmarks to pages, instantly search for the major terms or chapter titles, etc.
You can search our site for other versions of the Designing Science Presentations: A Visual Guide to Figures, Papers, Slides, Posters, and More 2nd Edition PDF ebook. You can also search for others PDF ebooks from publisher Academic Press, as well as from your favorite authors. We have thousands of online textbooks and course materials (mostly in PDF) that you can download immediately after purchase.
Note: e-textBooks do not come with access codes, CDs/DVDs, workbooks, and other supplemental items.
eBook Details:
Full title: Designing Science Presentations: A Visual Guide to Figures, Papers, Slides, Posters, and More 2nd Edition
Edition: 2nd
Copyright year: 2021
Publisher: Academic Press
Author: Matt Carter
ISBN: 9780128153772, 9781000215908
Format: PDF
Description of Designing Science Presentations: A Visual Guide to Figures, Papers, Slides, Posters, and More 2nd Edition:
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.
