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VIVEbiotech is a GMP Contract Development and Manufacturing Organization (CDMO) specialized in Lentiviral vectors.

VIVE is focused on the manufacture of Research, Preclinical toxicology and GMP-grade lentiviral vectors offering all the related services prior release by our Qualified Person.

Sealed as Excellence Centre by European Union, VIVE is currently working with Companies based both in Europe and USA being our main interest adapting to Customer requirements considering also planning and timelines related issues.

Additionally, VIVE has developed LENTISOMA´s technology, a non-Integrative Lentiviral replicative episomal vector.

Contact VIVEbiotech
+34 943 308 568
nelizalde@vivebiotech.com
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