Satisfies all needs for Early Clinical Trials including PM, Monitoring, Medical Writing and CDM/STAT
Clinical is supported by API Synthesis, Bioanalysis with small/large molecules, cell-based assays, biomarkers and Clinical Trial Supplies.
Infrastructure
Headcount: 295 employees (42% university graduates)
Bioanalytical Capacity: 1.305 m²
Bed capacity: 110 (including Site Gauting)
Inspections & Authorizations
GMP certified (1989)
GLP certified (1994)
ANVISA certified (2005)
License to work with genetically modified organisms (S1)
History
Established in 1979
Started as LAB, changed to AAI and since 2010 NUVISAN GmbH
Today, NUVISAN is a fully integrated CRO/CDMO
Working Fields & Specialties
In-house CPU with 140 beds including PM, Monitoring, Medical writing and CDM/STAT
Bioanalysis with small and large molecules, cell-based assays and Biomakers
Safety lab
Clinical Trial Supplies: GMP Manufacturing and Packaging Services
API Synthesis