Who we are
For the last 10 years we have developed and manufactured lentivirus under both EMA and FDA standards as an experienced leader in the field. The lentiviral vectors produced by VIVEbiotech are administered both ex vivo and in vivo to treat a range of disorders, including haematological and solid cancers, and rare diseases.
We are a Contract Development and Manufacturing Organization (CDMO) with over 50 biotech and pharmaceutical companies worldwide that have placed their trust in us.
A solid project with its own personality
Our roots are 100% Guipuzcoan. Since 2015 we have spearheaded the creation of an ecosystem in our region specialized in health-related biotechnology aimed at personalized precision medicine.
Our origins
Our stable international clients and large-scale projects allow us to consolidate our structure and continue to grow sustainably, positioning our company and our region at the forefront of the medicine of the future on a global level.
VIVEbiotech through the years
- US, European, Asian and Australian clients
- Compliance with EMA and FDA regulations
- GMP certification for clinical-grade release
- 7 clean rooms fully dedicated to lentivirus
- One of the few companies fully focused on lentiviral vectors
- Timely slot availability
- Growth investment secured in 2024
Project with a future
These are exciting times in the world of biotechnology and health, with realistic expectations for cures for many pathologies. VIVEbiotech is one of the players making this possible. In 2024 we secured a growth investment from Ampersand Capital Partners to expand lentiviral vector development and manufacturing capabilities.