pharma bio pharma

Pharma/ Bio Pharma Services

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 Vivotecnia, 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.



Please contact us to discuss your particular needs and goals.

Latest News


Safety Pharmacology Services

In Vivotecnia we want to get the most out of our animal facilities. That's why we have implemented the cardiovascular telemetry in dogs, using cutting-edge technology: The telemetry system provider...
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The innovative PYME certification

Vivotecnia has obtained the innovative PYME certification from the Ministry of Economy.
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AMESplus1 – OECD 471 Bacterial Reverse Mutation Test + Confirmation Test

Do you want to discard genetic damage of your products? request the Ames test setup by Vivotecnia, AMESplus1: Save time and money by doing the Standard AMES Test and the Confirmation Test all in one...
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