2025
Rogers JM . 2025. Maternally mediated developmental toxicity. In: Comprehensive Toxicology, 4th Edition. Elsevier. In Press (Sept 2025). Available online June 9, 2025 via Reference Module in Biomedical Sciences; doi: 10.1016/B978-0-323-95488-4.00280-1 .
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Topics: food additives , risk assessment
2024
Wikoff D , Fitch S . 2024. Systematic reviews and evidence-based methods in toxicology. In: Wexler P (ed), Encyclopedia of Toxicology. Elsevier, pp. 875–882.
Topics: evidence-based reviews , Systematic Review
Wikoff D , Fitch S . 2024. Evidence‐based methods in toxicology: Systematic review and systematic evidence mapping. Chapter 32 in: Paustenbach DJ (ed), Human and Ecological Risk Assessment: Theory and Practice, Third Edition, pp. 1133–1148. Wiley , ISBN: 978-1-119-74296-8.
Topics: Systematic Review
2023
Britt JK. 2023. Insect repellents (DEET) and others. In: Patty’s Industrial Hygiene and Toxicology. John Wiley & Sons; https://doi.org/10.1002/0471125474.tox140 .
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Topics: pesticides
2022
Henderson RG , Nguyen H. 2022. Pathways to the US supplement market: New dietary ingredient notification and Generally Recognized as Safe determination. Chapter 19 in: Ruthsatz M, Wong AW (eds), Nutrition, Health, and Disease: Regulatory Policy Matters. Regulatory Affairs Professionals Society, E-Book, 427 pp., ISBN: 978-1-947493-82-7.
Topics: Food science , nutrition
2021
Kimzey A , Mease K, Mounho-Zamora B, Wood M. 2021. 13. Biosimilar products—A review of past and current regulatory approval standards for preclinical safety studies. In: Translational Medicine : Optimising Preclinical Safety Evaluation of Biopharmaceuticals. CRC Press: Boca Raton, FL .
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Topics: regulatory toxicology
2019
Mihalchik-Burhans AL , Rogers EN. 2019. Considerations for leachables and extractables testing. In: Gad S (ed), Integrated Safety and Risk Assessment for Medical Devices and Combination Products, pp. 239–263. Springer .
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Topics: leachables
Mihalchik-Burhans AL , Sullivan DW. 2019. Bridging issues of route. In: Gad S (ed), Integrated Safety and Risk Assessment for Medical Devices and Combination Products, pp. 273–297. Springer .
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Topics: chemical safety assessment , pharmacokinetics , regulatory toxicology
2018
Kimzey AL , Piche M-S, Wood M , Weir AB, Lansita J. 2018. 11.19 – Immunophenotyping in drug development. In: Comprehensive Toxicology, 3rd Ed. Vol 11:399–427 .
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Topics: drug development
Fourches D, Williams AJ, Patlewicz G , Shah I, Grulke C, Wambaugh J, et al. 2018. Computational tools for ADMET profiling. Chapter 8 in: Ekins E (ed), Computational Toxicology: Risk Assessment for Chemicals, pp. 211–244. doi: 10.1002/9781119282594.ch8.