EMA receives application for conditional authorisation of first COVID-19 treatment in the EU pr011 June 09 / 2020 Tags conditional marketing authorisation rolling review human medicines committee Read more about EMA receives application for conditional authorisation of first COVID-19 treatment in the EU EMA has now received an application for conditional marketing authorisation (CMA) of the antiviral medicine remdesivir for the treatment of COVID-19 and has formally started its evaluation.