Italy
Regulation name: EU Falsified Medicines Directive
Serialization status: Deadline – February 9, 2025
Country population: 58,8 mln people
Market coding requirements: Bollino
NMVS provider (EU Only):
Alert management: Not required
Aggregation requirement: Not mandatory
Track & Trace requirement: No
Official governing body: The Italian Medicines Agency (AIFA) (https://www.aifa.gov.it/en/)
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