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BRUSSELS, Nov 26 (Reuters) - Europe's drugs watchdog said on
Thursday it expects to receive the first application for
conditional marketing approval for a COVID-19 vaccine "in the
coming days", the latest step towards making a shot available
outside the United States.
The European Medicines Agency (EMA) did not name the company
it expects to file the application, but Pfizer Inc and
BioNTEch are the most advanced in the regulatory
process among the three companies that have published late-stage
trial data for their vaccines.
(Reporting by Francesco Guarascio in Brussels;
Writing by Josephine Mason in London
Editing by David Goodman)
