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Searching on the web:
COMMISSION DELEGATED REGULATION (EU)
Online dispensing
Annual Report 2009
Withdrawal of the marketing authorization only for the certain strength of the product
Main changes in Slovak Drug Law - Clinical trials (human)
Duration of approval process 2010
Adverse event/reaction in a clinical trial - Reporting requirements in the Slovak Republic
№ 331 ACT of 23 June 2005 on state administration authorities in matters of drug precursors, and on amendments and additions to some laws
REGULATION (EU) No 1258/2013 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 20 November 2013 amending Regulation (EC) No 273/2004 on drug precursors
REGULATION (EU) No 1259/2013 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 20 November 2013 amending Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Community and third countries in drug precursors
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