The EuropeanMedicinesAgency has revealed a list of five cities that are preferred as its new location by staff after Brexit, following warnings of a public health disaster if EU leaders pick ...
announced today that the EuropeanMedicinesAgency (EMA) has accepted a Marketing Authorization Application for AVT03, a proposed biosimilar candidate to Prolia® and Xgeva® (denosumab).
The UK’s chief Brexit negotiator, minister David Davis will fight to keep the EuropeanMedicinesAgency in London, despite the country leaving the EU. The Financial Times has reported that the ...
The European Commission (EC) will decide in approximately two months. Last month, Novartis released new data from the ALITHIOS open-label extension study. Data show first-line Kesimpta (ofatumumab ...