Transcription of Commission Regulation (EU) No 712/2012 of 3 …
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Commission Regulation (EU) No 712/2012 of 3 …
L 209/4 EN Official Journal of the European Union Commission Regulation (EU) No 712/2012 . of 3 August 2012. amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance). THE EUROPEAN Commission , medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for Having regard to the Treaty on the Functioning of the European human and veterinary use and establishing a European Union, Medicines Agency, and Regulation (EC) No 1394/2007. on advanced therapy medicinal products (6), and the provisions of Directive 2010/84/EU of the European Having regard to Directive 2001/82/EC of the European Parliament and of the Council of 15 December 2010.
COMMISSION REGULATION (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of
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