Charles River Highlights Effectiveness of VCGs in Toxicology
Peer-reviewed evidence supports the use of Virtual Control Groups in nonclinical toxicology studies
“Virtual Control Groups show that scientific rigor and meaningful reductions in animal use are not mutually exclusive,” said Dr. Namandjé
Impact of VCGs
VCGs apply historical control data, advanced statistics, and AI-enabled analytics to digitally replace a portion of concurrent control animals in regulated safety studies. By reducing animal use and improving data interpretability, VCGs offer a modern, ethical, and scientifically robust alternative for developers seeking more efficient decision-making.
“Our focus has been on translating VCGs from concept to execution,” added
Virtual Control Groups help accelerate timelines, enhance data quality, and meet evolving regulatory expectations for the
- Up to 25% reduction in control group animal use where scientifically appropriate, without compromising regulatory-grade rigor
- Greater statistical power, particularly for detecting rare spontaneous findings that may otherwise obscure study outcomes
- More consistent interpretation, leveraging large, curated historical datasets to contextualize unexpected results
- Improved study efficiency, freeing resources and enabling teams to focus on higher-value scientific questions
Charles River brings deep toxicology expertise and a long-standing commitment to alternative methods, highlighted through the formation of their
Global Industry Collaboration
In 2025, Charles River joined the
This type of industry collaboration led to the European Medicines Agency’s recent draft qualification, focusing on the application of VCGs in dose-range finding (DRF) non-GLP repeated dose toxicity rat studies. This is an important step towards the regulatory acceptance of VCGs.
“Collaborating with the regulatory agencies is crucial as we progress validation work in alternatives like VCGs,” added Bumpus. “Partnering to design qualification standards for data-sets and define acceptable use cases early on will help build the industry’s confidence in VCGs and support their adoption once they are validated alternatives.”
Charles River remains committed to advancing the validation and acceptance of NAMs. Together with clients, regulators, and the industry, NAMs provide a foundation for a future where more patients gain access to life-saving treatments—safely, swiftly, and with reduced reliance on animal use in research where scientifically appropriate.
About the
About Charles River
Charles River provides essential products and services to help pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe accelerate their research and drug development efforts. Our dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development and safe manufacture of new therapies for the patients who need them. To learn more about our unique portfolio and breadth of services, visit www.criver.com.
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