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Clinical Trials
Clinical Trials Procedures
Comments to Commision Regulation proposal concerning the examination of variations in marketing authorisation and registration dossier
COMMISSION DELEGATED REGULATION (EU)
COMMISSION IMPLEMENTING REGULATION (EU) 2015/1013 of 25 June 2015 laying down rules in respect of Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and of Council Regulation (EC) No 111/2005 (drug precursors)
Commission regulation (EC) No 1277/2005
COMMISSION REGULATION (EC) No 297/2009 amending Regulation (EC) No 1277/2005
COMMISSION REGULATION (EU) No 225/2011 of 7 March 2011 amending Commission Regulation (EC) No 1277/2005 (drug precursors)
COMMISSION REGULATION (EU) No 225/2011 of 7 March 2011 amending Commission Regulation (EC) No 1277/2005 (drug precursors)
Committee for Medicinal Products
Communication in drug safety Approach of State Institute for Drug Control
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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
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