About us

Who we are

Who we are defines our purpose.

Preclinical regulatory CRO

Scroll down

Established – 2000

Founded in 2000, Vivotecnica was born with a clear vision: to offer preclinical studies with the highest scientific, ethical and regulatory standards.

Years of experience
+ 0
Studies performed  
+ 0

GLP

Certified since 2003 

Employees 
+ 0

In vivo

Toxicological studies experts 

Integrated approach

An independent preclinical CRO for scientific excellence

At Vivotecnia, each study we develop is supported by a multidisciplinary team of scientists, technicians and experts working under a rigorous quality system, accredited by international standards.

We are proud to offer solid scientific solutions that are also flexible and tailored to the real needs of each client. We understand that every project, every compound, and every assay requires a unique approach.

A team that believes in what it does.

A team that believes in what it does

Behind every study there are people committed to science, rigor and ethics. Our team is made up of highly qualified professionals who combine experience, passion and a collaborative approach. 

State-of-the-art infrastructure

State-of-the-art infrastructure

Vivotecnia has modern facilities in Madrid, equipped with state-of-the-art technology and a controlled environment that guarantees the reliability of the results and the safety of the procedures. 

International projection

International projection

We collaborate with companies from all over the world building close and transparent relationships without geographical barriers. Our proximity to Madrid International Airport makes us an easily accessible and reliable partner for international clients.

Committed to animal welfare and sustainability

Committed to animal welfare and sustainability

At Vivotecnia we do not understand research without ethics. We apply the principles of Replacement, Reduction and Refinement (the 3Rs) in all our processes, promoting practices that minimize the use of animals and guarantee their welfare. 

Excellence in quality and compliance 

Excellence in quality and compliance 

All our studies are conducted under strict Good Laboratory Practice (GLP) standards, which follow all international guidelines (OECD, ICH, and others). They are audited by independent Quality Assurance units and certified under ISO 9001:2015. Our digital systems ensure traceability, transparency, and regulatory compliance at every stage.

Active participation in the scientific community

Active participation in the scientific community

At Vivotecnia, we are actively involved in international scientific events and congresses, fostering continuous training for our team and promoting knowledge exchange with the academic world. This ongoing interaction positions us as an integral part of the scientific system, ensuring that our practices remain at the forefront of innovation and regulatory requirements.

Regulatory expertise

Your long-term scientific partner

At Vivotecnia, each study is supported by a multidisciplinary team of scientists, technicians, and experts working under a rigorous quality system, accredited by international standards such as GLP.

We are proud to offer solid scientific solutions that are also flexible and tailored to the real needs of each client. Beyond individual studies, we act as long-term partners, covering the different phases of development and evolving together with each project to ensure its success at every stage.

Who we are

If you are looking for a committed team,

with experience and scientific vision,
Vivotecnia is your ally in preclinical

toxicology.

We use cookies

We use cookies to improve your experience on this website. You may choose which types of cookies to allow and change your preferences at any time. Disabling cookies may impact your experience on this website. You can learn more by viewing our Cookie Policy.