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Regulatory Watch
  • Πέμπτη 11 Ιούν 2015
    Regulatory Watch
    0

    The EMA has informed that a number of changes have been made to the templates of the product information (Quality Review of Documents (QRD) templates) that accompany all medicines authorised for use in the European Union.

     
1 Αντικείμενα. Σελίδα 1/1