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About TOXPLUS

Founded in January 2020, TOXPLUS is a trusted partner for biotech and pharmaceutical companies seeking expert nonclinical drug development support. TOXPLUS specializes in pharmacology/toxicology support, study management, global study monitoring for both GLP and non-GLP studies, vendor audits, data review audits and regulatory writing support. With a commitment to quality and efficiency, TOXPLUS empowers clients to navigate the complexities of drug development with confidence. 

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Experience and Expertise

Reliable Nonclinical Support

The TOXPLUS Team brings decades of experience in nonclinical drug development, working closely with clients to provide expert guidance at every step. We have a comprehensive understanding of toxicology, study management, regulatory expectations, and the importance of data integrity in GLP and non-GLP pharmacology/toxicology studies. Whether you need expert oversight for your nonclinical program and/or guidance through complex requirements, TOXPLUS is here to support your success. 

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Your Trusted Nonclinical Partner

Our team brings decades of hands-on experience working with contract research organizations (CROs) across the globe. We understand the intricacies involved in partnering with a dependable CRO while navigating regulatory requirements, budget limitations, and ensuring data integrity. If you're looking for expert support for your upcoming study or program, TOXPLUS is here to assist you.

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