Before the implementation of Commission Delegated Regulation 2016/161 the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia calls on the marketing authorisation holders to provide information about product codes used in unique identifiers on medicinal products placed on the market in the Republic of Slovenia.
Marketing authorization holders shall forward the abovementioned information in the Excel document together with the following attributes:
- national identifier
- name of the medicinal product
Marketing authorization holders should also forward any changes of the product codes to the abovementioned e-mail address.