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About SIDC
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List of registered / announced medical devices, codes and economic operators from 1.1.2018
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Searching on the web:
Notification about the possibility to submit authorisation applications and related documents through the CESP Portal
Electronic Application Forms (eAFs) mandatory for all precedures from January 2016
Annual Report 2015
Slovak human and veterinary medicines agencies hosted the second meeting of the Heads of Medicines Agencies
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
Submission of the marketing authorisation applications via DC, MR procedures – national requirements
Annual Report 2016
Information on falsified medicines
Recall of medicinal products
Form for submitting clinical trial documents to the SIDC
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