Improving efficiency of approval process for new medicines in the EU

EMA

2 October 2024 - EMA and the European medicines regulatory network are working to further improve efficiency in the assessment and approval processes for new medicines in the European Union. 

The initiative aims to better manage the use of the network's expert resources, streamline assessment processes and encourage better and more comprehensive application dossiers from applicants at the time of initial submission. The overall objective of the initiative is to accelerate the availability of safe and effective treatments for patients.

Read EMA press release

Michael Wonder

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Michael Wonder

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Medicine , Europe , Regulation , Timelines