Pharma/ Biopharma Services
During pharmaceutical development at Vivotecnia, we help our clients to conduct preclinical, GLP-compliant general toxicology, genotoxicity, carcinogenicity, reproductive toxicity and safety pharmacology 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. Vivotecnia’s extensive service catalog means we can offer you anything from stand-alone studies to complete first-in-human or full pharmaceutical-development study packages.
Vivotecnia operates under rigorously enforced quality standards, tailoring our efforts to nearly any special procedures that may be requested or designing packages to meet the specific demands of each client and trial. We strive to attract and retain our clients through exceptional expertise at competitive prices. Our objective is cost-effective preclinical research services emphasizing fluid communication, punctuality and responsiveness.