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TOXPLUS
About CRO
TOXPLUS is a trusted partner for biotech and pharmaceutical companies seeking expert nonclinical drug development support. Founded in 2020, the company specializes in pharmacology and toxicology support, study management, global study monitoring (GLP and non-GLP), vendor and data review audits, and regulatory writing. With decades of experience in nonclinical research and a strong focus on data integrity, regulatory compliance, and quality, TOXPLUS helps clients advance their drug programs from preclinical studies to the clinic with confidence.
Technology & Expertise
At TOXPLUS, we specialize in Clinical Trials, Site Monitoring, Regulatory Affairs, Consulting, Preclinical Studies, Other Services. Our approach brings together protocol execution, site coordination, participant oversight, and study delivery; risk-based site oversight, source review, issue escalation, and follow-up; regulatory strategy, authority interactions, and submission planning; and connected specialist capabilities, enabling project teams to scale support as priorities and development stages change.
Core Services
Our service portfolio spans Clinical Trials, Site Monitoring, Regulatory Affairs, Consulting, Preclinical Studies, Other Services. TOXPLUS can coordinate trial planning, start-up, monitoring, and close-out support; monitoring activities spanning initiation through close-out; development-pathway advice, document preparation, and agency support; and connected specialist capabilities within a defined project structure designed around milestones, data needs, and operational priorities.
Accreditations & Compliance
Our public materials reference GLP. At TOXPLUS, the compliance package is aligned with the proposed scope of work. Accreditation status, regulatory coverage, and inspection evidence should be confirmed for the exact facility and service included in the proposal.
