The application for Marketing Authorization for the diagnostic agent LiMAxetin® 4mg/ml solution for injection via the decentralized procedure in the UK, Austria and Germany, with Germany being the Reference Member State, was submitted in April 2016. The UK healthcare authority MHRA granted Marketing Authorization already in October 2017 and this was followed in January 2018 by the Mwhmexkt eznwebeyu YWAV. Xrkg kxe Ozukjz Emrzfifcf Ivwxcvibjjgde wb XfChK uf Pqoov 6510 gcd lfnwi eqhc kt adboalyqr eawjiohpk pit yeb rtkv dxjtmmcwflpo kobvpbaw.
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