Pharmaceutical Analytical Solution from Early Stage to Commercialization

With three GMP- and one GLP-certified laboratories and more than 100 analytical experts across Europe, NUVISAN offers comprehensive bioanalytical and CMC services throughout the product life cycle, from early research and development to manufacturing and commercialization. Our laboratories undergo regular GMP inspections by local authorities and two of our labs have been inspected and approved by the FDA. As an active member of the ICH guideline team, NUVISAN is dedicated to leading the way in industry standards and innovation.

In addition to traditional pharmaceutical testing—encompassing chemical, physico-chemical, and mechanical testing of raw materials, APIs, and finished drugs (small and large molecules, biologics), as well as batch release overseen by a Qualified Person (QP)—we assist our customers with analytical method development, method validation, ICH stability studies (including controlled storage), and photostability studies.

NUVISAN is committed to building strong and reliable partnerships with our global clients, spanning the pharmaceutical, biotechnology, and veterinary industries, as well as research institutions. Our services are designed to help bring safe and effective human and veterinary medicines to market.