At Vivotecnia we help our clients to conduct preclinical, GLP-compliant, general toxicology studies to evaluate the safety of new drug candidates. This process adheres to international regulatory requirements and submission requirements for clinical trials or marketing authorization.
Our general toxicology services comprise anything from non-GLP dose-range-finding studies to subchronic and chronic toxicology studies in rodent and nonrodent models. This along with Inocencia’s comprehensive service catalog means that we can offer you anything from stand-alone studies to complete first-in-human or full development study packages.
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Client Success Team (CRM),
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