Advancing NAMs for Risk Assessment: Perspectives from SOT 2025 
Paul Locke Paul Locke

Advancing NAMs for Risk Assessment: Perspectives from SOT 2025 

By Breanne Kincaid | April 17th, 2025

Together, these presentations illustrate a clear shift towards integrated, mechanistically informed risk assessment strategies that reduce the number of animals required to generate toxicity data—paving the way for regulatory frameworks that are both scientifically robust and economically sustainable.”

Image by Breanne Kincaid

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Organoid’s Potential to Advance Low Dose Research
Paul Locke Paul Locke

Organoid’s Potential to Advance Low Dose Research

By Loza Taye | April 3rd, 2025

Organoids will have an increasingly important role in shaping our understanding of radiation biology and in the development of policies and medical practices concerning radiation exposure.”

Image by aislan13

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The Utility of an Intra-Agency NAM Office
Paul Locke Paul Locke

The Utility of an Intra-Agency NAM Office

By Breanne Kincaid | January 10th, 2025

“…the FDA’s NAM office represents a strategic evolution in integrating innovative methodologies into regulatory science. While it complements ICCVAM’s mission, its intra-agency focus and regulatory authority position it to drive faster, more context-specific advancements in risk assessment.“

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Guest Blog: Swiss Court Prohibits Zebra Finch Experiment
Paul Locke Paul Locke

Guest Blog: Swiss Court Prohibits Zebra Finch Experiment

By Katerina Stoykova and Nicole Lüthi | October 17th 2024

“The harm-benefit analysis is a legal requirement under Swiss experimentation law, stipulating that animal experiments are only allowed if the anticipated benefits outweigh the stress inflicted on the animals. The more severe the stress caused by an experiment, the greater the expected benefit must be to justify it.”

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Regulation Updates in China
Paul Locke Paul Locke

Regulation Updates in China

By Yiguang Zhu and Zachary Leibowitz | August 22nd, 2024

“A wave of regulatory updates in China is reshaping the landscape of the field of animal testing, challenging long-standing practices and opening doors to innovative non-animal alternatives.”

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One Year Anniversary of the Tox Blog
Paul Locke Paul Locke

One Year Anniversary of the Tox Blog

By Loza Taye | August 22nd, 2024

“We aim to promote better science and support the transition towards more humane and effective methods by covering legislative developments, innovative research techniques, and legal considerations…”

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Meeting the Requirements of the AWA Workshop Recap
Paul Locke Paul Locke

Meeting the Requirements of the AWA Workshop Recap

By Loza Taye | July 25th, 2024

“...AWIC hosted a workshop to promote successful research planning that meets the AWA requirements. Key takeaways from this event included the importance of early planning, cost considerations, effective search strategies, cultivating empathy, embracing progress, and enhancing proficiency in alternatives research.”

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MPS World Summit 2024 Recap
Paul Locke Paul Locke

MPS World Summit 2024 Recap

By Breanne Kincaid & Yiguang Zhu | July 11th, 2024

“In attending the MPS World Summit and other conferences and webinars, it is increasingly clear that MPS developers and end-users would all benefit from clearly enumerated regulatory requirements describing what benchmarks must be met in order for MPS data to be accepted for particular use contexts.”

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