Vivotecnia
Security and confidence in every study
Preclinical regulatory CRO
Established – 2000
Our commitment
At Vivotecnia, we perform in vivo and in vitro preclinical studies to ensure the safety of new compounds before their use in humans. We specialize in general toxicology, safety pharmacology, bioanalytical analysis, inhalation, and reproduction studies.
Our Experience
With more than 25 years of experience, Vivotecnia offers customized studies in compliance with global regulations, ensuring reliable and applicable results for the development of innovative products.
We evaluate the safety and toxicity of compounds administered by inhalation through controlled exposure systems, recreating real conditions of use.
We assess the impact of substances on fertility, embryo development, and reproductive health, in accordance with regulatory guidelines such as OECD 414, 421, 422, and 443. For pharmaceutical development, we include Segment I, Segment II , and Segment III, following ICH guidelines (e.g., ICH S5).
We design specific studies for biotechnological products, including bioanalysis, stability and validation of complex formulations.
We support the development of innovative therapies such as ATMPs through tailored preclinical trials focused on demonstrating their safety and efficacy.
Our ethics
At Vivotecnia, we believe in responsible research. We apply the principles of the 3Rs to minimise the use of animal models and guarantee their welfare, complying with international ethical standards in experimentation.
Replace
Animal studies with non-animal methods
if not possible
Reduce
Animal studies to minimum required and necessary
in addtion
Refine
Practices to minimize stress of study animals
That is why we work under strict regulatory protocols and in collaboration with international organisations that guarantee transparency and excellence in each project.
Project Management
Each project is unique, which is why we tailor our studies to the specific needs of every client. From preclinical development to comprehensive toxicological evaluation, we provide personalized advice and reliable results.
Our team of Study Directors will accompany you throughout the entire process, ensuring direct communication with our experts at every stage.
Definition of objectives, selection of the appropriate model and signing of the study plan.
Development of the study under controlled conditions, daily monitoring and data collection
Bioanalysis, formulation, and sample validation using advanced technologies, with data collection managed through Provantis, the leading system in the preclinical world.
QA oversight throughout the entire process: from audit and final report generation to GLP-compliant archiving, with QA accompanying each project from the very beginning.
Tell us more about your project!
If you are looking for a committed team,
with experience and scientific vision,
Vivotecnia is your partner in preclinical
toxicology requitement.
