Ireland Regulation name: EU Falsified Medicines Directive Serialization status: Active Country population: 5 mln people Market coding requirements: GTIN, Expiry Date, Batch Number, Serial Number NMVS provider (EU Only): IMVO Alert management: Yes – required Aggregation requirement: Not mandatory Track & Trace requirement: Not mandatory Official governing body: Health Products Regulatory Authority (HPRA) (https://www.hpra.ie/)