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165,79 €
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Key Statistical Concepts in Clinical Trials for Pharma
Key Statistical Concepts in Clinical Trials for Pharma
149,21
165,79 €
  • We will send in 10–14 business days.
This Brief discusses key statistical concepts that facilitate the inferential analysis of data collected from a group of individuals participating in a pharmaceutical clinical trial, the estimation of their clinical significance in the general population of individuals likely to be prescribed the drug if approved, and the related decision-making that occurs at both the public health level (by regulatory agencies when deciding whether or not to approve a new drug for marketing) and the individua…
  • Publisher:
  • ISBN-10: 1461416612
  • ISBN-13: 9781461416616
  • Format: 15.6 x 23.4 x 0.4 cm, softcover
  • Language: English
  • SAVE -10% with code: EXTRA

Key Statistical Concepts in Clinical Trials for Pharma (e-book) (used book) | bookbook.eu

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This Brief discusses key statistical concepts that facilitate the inferential analysis of data collected from a group of individuals participating in a pharmaceutical clinical trial, the estimation of their clinical significance in the general population of individuals likely to be prescribed the drug if approved, and the related decision-making that occurs at both the public health level (by regulatory agencies when deciding whether or not to approve a new drug for marketing) and the individual patient level (by physicians and their patients when deciding whether or not the patient should be prescribed a drug that is on the market). These concepts include drug safety and efficacy, statistical significance, clinical significance, and benefit-risk balance.

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  • Author: J Rick Turner
  • Publisher:
  • ISBN-10: 1461416612
  • ISBN-13: 9781461416616
  • Format: 15.6 x 23.4 x 0.4 cm, softcover
  • Language: English English

This Brief discusses key statistical concepts that facilitate the inferential analysis of data collected from a group of individuals participating in a pharmaceutical clinical trial, the estimation of their clinical significance in the general population of individuals likely to be prescribed the drug if approved, and the related decision-making that occurs at both the public health level (by regulatory agencies when deciding whether or not to approve a new drug for marketing) and the individual patient level (by physicians and their patients when deciding whether or not the patient should be prescribed a drug that is on the market). These concepts include drug safety and efficacy, statistical significance, clinical significance, and benefit-risk balance.

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