European regulator seeks to speed up approvals

3 October 2024

The European Medicines Agency (EMA) and the European medicines regulatory network are working to speed up the approval of new medicines.

The agency has said it wants to improve the use of expert resources and to streamline the assessment process, tackling long-standing inefficiencies.

A key focus of the reforms is the need to improve the predictability of submissions for marketing authorisation applications. In 2023, only 35% of MAAs were submitted on time, according to EMA data.

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