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Validation of Alternative Methods for Toxicity Testing

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Cover of 'Validation of Alternative Methods for Toxicity Testing'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction.
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    Chapter 2 Validation in Support of Internationally Harmonised OECD Test Guidelines for Assessing the Safety of Chemicals.
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    Chapter 3 Regulatory Acceptance of Alternative Methods in the Development and Approval of Pharmaceuticals.
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    Chapter 4 Validation of Alternative In Vitro Methods to Animal Testing: Concepts, Challenges, Processes and Tools.
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    Chapter 5 Practical Aspects of Designing and Conducting Validation Studies Involving Multi-study Trials.
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    Chapter 6 Validation of Computational Methods.
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    Chapter 7 Implementation of New Test Methods into Practical Testing.
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    Chapter 8 Pathway Based Toxicology and Fit-for-Purpose Assays.
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    Chapter 9 Evidence-Based Toxicology.
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    Chapter 10 Validation of Transcriptomics-Based In Vitro Methods.
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    Chapter 11 Ensuring the Quality of Stem Cell-Derived In Vitro Models for Toxicity Testing.
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    Chapter 12 Validation of Bioreactor and Human-on-a-Chip Devices for Chemical Safety Assessment.
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    Chapter 13 Integrated Approaches to Testing and Assessment.
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    Chapter 14 International Harmonization and Cooperation in the Validation of Alternative Methods.
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    Chapter 15 Evolving the Principles and Practice of Validation for New Alternative Approaches to Toxicity Testing.
Attention for Chapter 1: Introduction.
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Chapter title
Introduction.
Chapter number 1
Book title
Validation of Alternative Methods for Toxicity Testing
Published in
Advances in experimental medicine and biology, September 2016
DOI 10.1007/978-3-319-33826-2_1
Pubmed ID
Book ISBNs
978-3-31-933824-8, 978-3-31-933826-2
Authors

Chantra Eskes, Maurice Whelan

Editors

Chantra Eskes, Maurice Whelan

Abstract

Alternative approaches to animal testing are gaining momentum with an increasing number of test methods obtaining international acceptance, thanks in large part to the validation efforts conducted on these assays. The principles and process of validation were first established in the 1990s in Europe and USA, and further gained international recognition ensuring the broader acceptance of alternative test methods at a regulatory level. If these principles were successful in pioneering the regulatory acceptance of alternative methods for less complex endpoints, an evolution of concepts is needed to embrace emerging technologies and the increased complexity of endpoints. Innovative concepts and approaches of scientific validation can help to ensure the continued regulatory and international acceptance of novel alternative methods and technologies for toxicity testing such as human-based in vitro models derived from induced pluripotent stem cells and significant advances in bioengineering. This chapter provides a historical overview of the establishment and evolution of the principles of the scientific validation of alternative methods for toxicity testing as well as the challenges and opportunities for adapting those principles to keep pace with scientific progress whilst ensuring human safety and best serve the needs of society.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 33%
Student > Bachelor 1 17%
Lecturer 1 17%
Student > Doctoral Student 1 17%
Unknown 1 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 17%
Business, Management and Accounting 1 17%
Agricultural and Biological Sciences 1 17%
Economics, Econometrics and Finance 1 17%
Medicine and Dentistry 1 17%
Other 0 0%
Unknown 1 17%