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Drug Safety Evaluation (Pharmaceutical Development Series) [9781119755852]

Hardcover
SKU: 9781119755852
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Format Sturdy and long-lasting. Ideal for libraries and classrooms, and a polished choice for corporate gifts, leadership programs, or event takeaways.

Price $354.95

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Overview

Drug Safety Evluation

Comprehensive and practical guide presenting a roadmap for safety assessment as an integral part of the development of drugs and therapeutics

This fourth edition of Drug Safety Evaluation maintains the central objective of presenting an all-inclusive practical guide for those who are responsible for ensuring the safety of drugs and biologics to patients, healthcare providers, those involved in the manufacture of medicinal products, and all those who need to understand how the safety of these products is evaluated and shepherding valuable candidates to market.

Individual chapters address specific approaches to evaluation hazards, including problems that are encountered and their solutions. Also covered are the scientific and philosophical bases for evaluation of specific concerns (e.g., carcinogenicity, development toxicity, etc.) to provide both understanding and guidance for approaching the new problems that have come to face both our society and the new challenges they brought.

The many changes in regulatory requirements, pharmaceutical development, technology, and the effects of Covid on our society and science have required both extensive revision to every chapter and the addition of four new chapters.

Specific sample topics covered in Drug Safety Evaluation include:

  • The drug development process and the global pharmaceutical marketplace and regulation of human pharmaceutical safety
  • Sources of information for consideration in study and program design and in safety evaluation
  • Electronic records, reporting and submission, screens in safety and hazard assessment, and formulations, routes, and dosage regimens
  • Mechanisms and endpoints of drug toxicity, pilot toxicity testing in drug safety evaluation, and repeat dose toxicity
  • Genotoxicity, QSAR tools for drug safety, toxicogenomics, nonrodent animal studies, and developmental and reproductive toxicity testing
  • An appendix which provides an up to date guide to CROs for conducting studies

Drug Safety Evaluation was written specifically for the pharmaceutical and biotechnology industries, including scientists, consultants, and academics, to show a utilitarian yet scientifically valid path to the everyday challenges of safety evaluation and the problem solving that is required in drug discovery and development.



The book, Drug Safety Evaluation (Pharmaceutical Development Series) [Bulk, Wholesale, Quantity] ISBN#9781119755852 in Hardcover by Shayne Cox Gad, Dexter W. Sullivan, Jr. may be ordered in bulk quantities. Minimum starts at 25 copies. Availability based on publisher status and quantity being ordered.

Details

Author:
Shayne Cox Gad
Format:
Hardcover
Publication Date:
01/12/2023
ISBN-13:
9781119755852
Pages:
992
Publisher:
Wiley

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