pharmaceutical development

Pharma/ Biopharma Services  

During pharmaceutical development at Vivotecnia, we help the companies that trust in us to conduct preclinical, GLP-compliant general toxicology, genotoxicity, carcinogenicity, reproductive toxicity and safety pharmacology studies to evaluate the safety of new promising drugs. We work with different species of animals, from mice to dogs, depending on the type of study we are working on. 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. Through the animal studies we offer, it may be possible to find drugs in the future that have not been used in humans to date.

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 our trusts and trials. We strive to attract and retain them through exceptional expertise at competitive prices. Our objective is cost-effective preclinical research pharma services emphasizing fluid communication, punctuality and responsiveness.  

If you are looking for a pharma research company that can help you with your development, do not hesitate in contacting us for any further questions or information you require.

pharmaceutical development


    For more information or a formal quotation, please send us a message and we will contact you as soon as possible.