The base register of drug products is a register maintained by Fimea concerning licenced drugs and fixed-term products under a special licence. The register is updated twice a month.
It contains information on the identification, classification, medicinal substance and packaging of a drug product and the necessary codes for the prescription condition, ATC, form and container of a drug. For the fi ...
The register is meant for organisations responsible for purchases, distribution and sale of drug products and for healthcare organisations providing prescriptions. The customer must have IT knowledge in order to process the files.