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25. September 2017

Submission of the marketing authorisation application via DCP, MRP

Submission of the marketing authorisation application via national procedure

23. May 2017

Corrigendum to Commision Delegated Regulation (EU) 2015/1011 of 24 April 2015 supplementig Regulation (EC) No 273/2004 of the European Parliament and of the Coucil on drug precursors and Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors, and repealing Commision Regulation (EC) No 1277/2005

8. December 2016

Slovak human and veterinary medicines agencies hosted the second meeting of the Heads of Medicines Agencies

10. November 2016

SIDC as RMS

9. November 2016

In October, the SIDC presidency meetings focused on medical devices issues and public relations

23. September 2016

Announcement of a maintenance of the information system of SIDC

12. September 2016

The Heads of Medicines Agencies was held in Bratislava