NUVISAN holds a Manufacturing and Import License for Human and Veterinary Investigational Medicinal Products including corresponding GMP certificate, as well as a Controlled Drug License.
We provide these GMP services in 2 sites located in Europe. The sites are complementary and act as mutual back-ups to enabling the desired flexibility and reactivity in the services provided.
The Clinical Trial Supplies (CTS) department supports our clients by supplying medicinal products (IMP and standardized lab kits) for use in clinical trials, from Phases I – IV.
All necessary steps for importing, manufacturing, primary and secondary packaging are handled by the CTS department of NUVISAN, including labelling (and re-labelling), QP certification by an EU Qualified Person (QP), distribution and destruction of investigational medicinal products (IMP) and comparators. Either as a full service or customized to client’s needs.