All GMP activities are done under the supervision of our EU Qualified Persons (QP) on our two GMP facilities. Our QPs are experienced and trained to review, audit and release all types of finished products (oral, topical, sterile, biological drugs…). Our Team is able to support for both commercial products and clinical trial use.
To support clients with interest of conducting clinical trials in Europe, NUVISAN provides consulting and realization of performance or qualification audits world-wide. Thus, QP declaration and audit of manufacturing sites are proposed to our clients either for specific needs either part of global projects involving manufacturing, primary and secondary packaging services.