At TOXPLUS, our mission is to instill confidence in your nonclinical programs by providing comprehensive and reliable operational support while also providing additional support in the areas of toxicology and regulatory writing. We collaborate with your team to ensure nonclinical studies are conducted with the utmost ethical integrity, regulatory compliance, and robust scientific principles. 

Backed by decades of experience in the industry and across the globe, we work with clients to develop large and small molecules from lead candidate selection to regulatory submissions. We have experience in nonclinical studies across all animal species, and the complexities of various routes of exposure, dosing frequencies, and durations. Our comprehensive knowledge allows us to support clients at every stage, ensuring studies are conducted with precision and adherence to industry standards. Whether you need guidance on study design, regulatory strategy, or data interpretation, we provide the strategic expertise necessary to advance your program efficiently and with confidence.

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TOXPLUS is committed to providing the critical support and knowledge needed to advance your nonclinical program to the clinic.