Nuvisan manages comprehensive logistics services for clinical trials, including the importation of test products, sourcing of comparators and ancillary materials and global supply chain strategy. This involves coordinating qualified courier services and strategically located depots to help ensure timely, compliant and secure delivery of clinical trial materials across multiple regions.
Expertise in global distribution management enables us to minimise both product quantities and timelines. Distribution manuals are created to outline all necessary documentation, IRT interaction, courier and depot information. Our broad network of qualified couriers and depots helps ensure that your global supply chain is efficiently organised, and your product will arrive in due time at the clinical site.
Nuvisan provides secure storage solutions for controlled drugs, helping ensure compliance with stringent regulatory requirements for handling and storing such materials. The storage areas are specifically designed to meet GxP standards, with restricted access to authorised personnel only, helping ensure maximum security and prevent unauthorised handling. These facilities are equipped with 24/7 surveillance and environmental monitoring to maintain appropriate temperature, humidity and light conditions, which are crucial for the integrity of controlled substances.
Nuvisan’s overall GMP area are access controlled, qualified and temperature monitored. Qualified storage capacities for ambient, 2-8°C, -20°C and -80°C are available. The storage areas are organised and clearly labeled for easy tracking, helping ensure traceability and compliance with regulatory guidelines. Comprehensive inventory management systems support secure storage, retrieval and documentation of all materials.