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EMA Begins Evaluation of Novavax’ COVID-19 Vaccine

Nuvaxovid assessment will proceed under an accelerated timeline, with an opinion issued potentially within weeks.

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By: Kristin Brooks

Managing Editor, Contract Pharma

Novavax, Inc. announced that European Medicines Agency (EMA) has begun its evaluation of an application for conditional marketing authorization (CMA) for its COVID-19 vaccine, which will be marketed in the EU as Nuvaxovid.   “Today’s announcement from EMA brings Novavax another step closer to our goal of ensuring broad global access to our protein-based COVID-19 vaccine across Europe,” said Stanley C. Erck, President and Chief Executive Officer, Novavax. “Novavax looks ...

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