Statistical Thinking for Non-Statisticians in Drug Regulation

Nonfiction, Health & Well Being, Medical, Medical Science, Pharmacology
Cover of the book Statistical Thinking for Non-Statisticians in Drug Regulation by Richard Kay, Wiley
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart
Author: Richard Kay ISBN: 9781118702352
Publisher: Wiley Publication: May 20, 2013
Imprint: Wiley-Interscience Language: English
Author: Richard Kay
ISBN: 9781118702352
Publisher: Wiley
Publication: May 20, 2013
Imprint: Wiley-Interscience
Language: English

Written by a well-known lecturer and consultant to the pharmaceutical industry, this book focuses on the pharmaceutical non-statistician working within a very strict regulatory environment. Statistical Thinking for Clinical Trials in Drug Regulation presents the concepts and statistical thinking behind medical studies with a direct connection to the regulatory environment so that readers can be clear where the statistical methodology fits in with industry requirements. Pharmaceutical-related examples are used throughout to set the information in context. As a result, this book provides a detailed overview of the statistical aspects of the design, conduct, analysis and presentation of data from clinical trials within drug regulation.

Statistical Thinking for Clinical Trials in Drug Regulation:

  • Assists pharmaceutical personnel in communicating effectively with statisticians using statistical language
  • Improves the ability to read and understand statistical methodology in papers and reports and to critically appraise that methodology
  • Helps to understand the statistical aspects of the regulatory framework better quoting extensively from regulatory guidelines issued by the EMEA (European Medicines Evaluation Agency), ICH (International Committee on Harmonization and the FDA (Food and Drug Administration)
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

Written by a well-known lecturer and consultant to the pharmaceutical industry, this book focuses on the pharmaceutical non-statistician working within a very strict regulatory environment. Statistical Thinking for Clinical Trials in Drug Regulation presents the concepts and statistical thinking behind medical studies with a direct connection to the regulatory environment so that readers can be clear where the statistical methodology fits in with industry requirements. Pharmaceutical-related examples are used throughout to set the information in context. As a result, this book provides a detailed overview of the statistical aspects of the design, conduct, analysis and presentation of data from clinical trials within drug regulation.

Statistical Thinking for Clinical Trials in Drug Regulation:

More books from Wiley

Cover of the book Wildlife Search and Rescue by Richard Kay
Cover of the book Hydrogen Exchange Mass Spectrometry of Proteins by Richard Kay
Cover of the book Investing In Islamic Funds by Richard Kay
Cover of the book A Foreign Exchange Primer by Richard Kay
Cover of the book Small Animal Toxicology Essentials by Richard Kay
Cover of the book A History of Babylon, 2200 BC - AD 75 by Richard Kay
Cover of the book Samsung Galaxy Tab S For Dummies by Richard Kay
Cover of the book The Use and Misuse of Psychiatric Drugs by Richard Kay
Cover of the book Developing Core Literacy Proficiencies, Grade 6 by Richard Kay
Cover of the book Principles and Practice of Mixtures Toxicology by Richard Kay
Cover of the book The Daily Trading Coach by Richard Kay
Cover of the book Society of Fear by Richard Kay
Cover of the book Laboratory Astrochemistry by Richard Kay
Cover of the book Penetration Testing Essentials by Richard Kay
Cover of the book What You Need to Know about Project Management by Richard Kay
We use our own "cookies" and third party cookies to improve services and to see statistical information. By using this website, you agree to our Privacy Policy