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The Latvian Medicines Verification Organization prepared weekly progress reports on regulatory compliance, system readiness and user connection activity in Latvia.

Meetings of work groups for two days in order to assess the current results and to plan further progress of the project of medicines verification system

Information in the labelling text shall be renewed for medicinal products, which in accordance with the requirements of Article 54a of the Directive 2001/83/EC, shall bear the safety features