The European Medicines Agency provided 66 positive opinions in 2019, with approval granted to a total of 30 new active substances.
The details were published in the EMA’s highlights document for the year, which also includes an overview of its key recommendations in 2019 on the authorization and safety monitoring of medicines.
These results compare with the US regulator’s total of 48 positive decisions, from the Center for Biologics Evaluation and Research (CDER).
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