SIDC: English version

Medicinal Product and Medical Devices Recall

25.9.2017
Submission of the marketing authorisation application via DCP, MRP

Submission of the marketing authorisation application via national procedure
23.5.2017
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
8.12.2016
Slovak human and veterinary medicines agencies hosted the second meeting of the Heads of Medicines Agencies
10.11.2016
SIDC as RMS
9.11.2016
In October, the SIDC presidency meetings focused on medical devices issues and public relations
23.9.2016
Announcement of a maintenance of the information system of SIDC
12.9.2016
The Heads of Medicines Agencies was held in Bratislava
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