Sweden Regulation name: EU Falsified Medicines Directive Serialization status: Active Country population: 10,6 mln people Market coding requirements: GTIN, Expiry Date, Batch Number, Serial Number NMVS provider (EU Only): E-vis Alert management: Yes – required Aggregation requirement: Not mandatory Track & Trace requirement: Not mandatory Official governing body: The Swedish Medical Products Agency (https://www.lakemedelsverket.se/en)