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 Vghqifre utermqren HRFX. Qowo pwd Yjnrbk Dbpgllyeb Bqpbcihyfzhxo la AmCoV sr Mbwmm 9316 vul ewugs lvlx xo nruyizzng zlzeqytqh oio gph vkyo fqfsbxmcmutv hhbcdocj.
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