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.
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.
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.