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TOXPLUS Monitoring is a specialized contract research organization providing global nonclinical operations support to biotech and pharmaceutical companies. Their services include study management, study monitoring for GLP and non-GLP studies, vendor audits/qualifications, toxicology support, data review audits, and regulatory writing. They work with all drug modalities—including small molecules, biologics, cell therapies, and gene therapies—across early to late-stage drug development. The company does not develop its own therapeutics or maintain an internal clinical pipeline.
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