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CRC Press Quantitative Drug Safety and Benefit Risk Evaluation

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Description

This professional text from the Chapman and Hall/CRC Biostatistics Series provides an in-depth look at quantitative methodologies and processes for safety monitoring. As pharmacovigilance shifts from individual adverse event reports toward aggregate analysis, this book addresses the need to better understand the scope of product risks. It covers safety monitoring methodologies including global trends and regional initiatives. Designed for a multidisciplinary audience, the content is written to be accessible to both statisticians and safety scientists with a quantitative interest. It serves as a bridge in knowledge for professionals working in drug safety and benefit-risk evaluation through practical and cross-disciplinary approaches.

Key Features

Covers quantitative methodologies and processes for safety monitoring and ongoing benefit risk evaluation.

Explores safety monitoring methodologies including both global trends and regional initiatives.

Addresses the industry shift from individual adverse event reports to aggregate analysis for product risk understanding.

Provides a bridge in knowledge between statisticians and safety scientists with a quantitative interest.

Part of the Chapman and Hall/CRC Biostatistics Series for professional medical and healthcare practitioners.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
29 December 2021
Listed Since
31 July 2021

Barcode

No barcode data available

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