NUVISAN specializes in radiolabeling APIs with different isotopes including stable isotope labeled NCEs (D, 13C, 15N) and radioactive labeled NCEs or peptides (3H, 14C), offer customized synthesis and analytical services, and have the expertise to support your preclinical and clinical studies.
The NUVISAN group is a Contract Research Organization (CRO) and Contract Manufacturing Organization (CDMO) with its headquarters in Neu-Ulm and six sites in Germany and France (Neu-Ulm, Berlin, Grafing, Gauting, Waltrop and Sophia-Antipolis) in addition to monitoring activities with offices in Argentina, Peru and Brazil as well as in the USA.
NUVISAN offers integrated and coupled services and solutions along the drug development value chain from target identification to the patient with all supporting services (DMPK, GMP synthesis, formulation development and analysis, bioanalysis, Phase 1 CPU, clinical trial supplies and monitoring).
Having a proven track record to include over 40 years of continuous service is a testimony to the operational excellence and the experience of our 1.000 highly qualified employees.
Years of experience
Sites across Europe
High educated motivated people
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
Clinical Trial Supplies: GMP Manufacturing and Packaging Services
Pharmaceutical | Clinical | Bioanalytical
Drug discovery team with extensive expertise in Pharma R&D
Fully integrated research functions across the whole discovery value chain
Broad coverage for indications / disease areas including focus on Oncology
Molecule research with strong foothold for small molecules with access to a high quality compound library
Lead Discovery | Life Science Chemistry | Therapeutic Research | Preclinical Compund Profiling | Library
Specialists in topical formulations for drugs and cosmetics including all types of semi-solid formulations
Chemistry: API synthesis, process development & GMP manufacturing
Clinical Trial Supplies
Quality Assurance & Regulatory Affairs
Formulation Development | Chemistry | Pharmaceutical | Bionanalytical
In-house CPU with 30 beds including PM, Monitoring, Medical writing and CDM/STAT
Specialist in respiratory indications
Pharmaceutical analysis including small/ large molecules and pharmaceutical antibodies
TDS and other Polymer based drug delivery formulations
Stability testing for all kind of conditions
Bioanalysis with respect to discovery and GLP bioanalysis with fast turnaround times
Mass Spectometry with license to handle radioactivity: human mass balance studies can be supported
In-vitro & In-vivo DMPK
Metabolite Profiling and Identification
Radiosynthesis/Isotope Labelling & QWBA
Preclinical | Bioanalytical