EMA's Guido Rasi fears loss of expertise from Brexit but hopes for common framework with FDA
Guido Rasi, executive director of the European Medicines Agency (EMA), has seen some huge steps being taken by the regulator since he first took on the role in 2011.
That includes in how the agency interacts with pharma, health technology assessment (HTA) bodies and patients, the speed in which it can assess innovative medicines, and in data sharing and working closely with the US Food and Drug Administration (FDA).
"What is needed anywhere is to introduce the environment that we have built in 20 years in London"
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