European Distribution Products (EDP)

The European Distribution or parallel import consists in a medicine authorized in one-member state can be marketed in another member state, in which it is also authorized. For this, it is necessary to obtain a Parallel Import Authorization, granted by the AEMPS or EMA, in the case of being a specialty with European registration.
The EDP have a national code different from that of the national presentation assigned by the AEMPS, and the product is reconditioned following the regulations of the country of commercialization.
To satisfy an optimal quality level and guarantee the safety and traceability of EDPs, Difarmed rigorously applies Good Manufacturing Practices (GMPs) and Good Distribution Practices (GDPs).
We comply with the Delegated Regulation (EU) 2016/161 and the requirements for serialization with the unique identifier and the anti-tamper devices in the secondary packaging.