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European Medicines Regulation

European Medicines Regulation, Total:3 items.

In the international standard classification, European Medicines Regulation involves: .

EU/EC - European Union/Commission Legislative Documents, European Medicines Regulation

• COM(2016) 498 FINAL-2016 REPORT FROM THE COMMISSION Pharmacovigilance related activities of Member States and the European Medicines Agency concerning medicinal products for human use (2012 – 2014) (SWD(2016) 284 final)

IX-EU/EC, European Medicines Regulation

• COM(2013) 472 FINAL-2013 Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on fees payable to the European Medicines Agency for the conduct of pharmacovigilance activities in respect of medicinal products for human use (2013/0222 (COD); Text with EEA relevan
• COM(2008) 664 FINAL-2008 Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medic

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