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At Vivotecnia we help our clients to conduct preclinical GLP-compliant general toxicology, genotoxicity, carcinogenicity, reproductive toxicity and safety pharmacology studies to evaluate safety of new drug candidates adhering to international regulatory requirements and filling your regulatory submission for clinical trial or marketing authorisation. The wide range of services provided by Viviotecnia, enable us to offer you from stand-alone studies to “First Time In Human” or “Full Development” complete study packages.

Vivotecnia operates under rigorously enforced quality standards while remaining flexible. We can tailor our efforts to nearly any special procedures that are requested or designed to meet the specific demands of each client and trial. We strive to attract and retain our clients through exceptional expertise at competitive pricing, strong communication, timeliness, responsive and cost-effective preclinical research services.

 

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Please contact us to discuss your particular needs and goals.




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