psn is experienced in the handling of clinical trials supplies in all countries covered.
In particular, psn has developed a special department which holds a good manufacturing practice (GMP) authorisation issued by the Danish Medicines Agency for import, stock, randomisation, labelling, repackaging and distribution of clinical trials supplies.
Its clinical trial supply department has developed a tracking system that will accurately track all supplies received and dispatched. The system can even record each individual container dispensed to patients.
For long-term clinical trials with large numbers of subjects, psn has developed a drug request system for re-supplies. This system is backed by a Drug Receipt Confirmation system via fax-in compliance with good clinical practice (GCP) for drug accountability. Periodic progress reports can be issued as required by the sponsor and can be made as detailed as necessary.