The new effort combines adaptive platform trial design, AI-enabled site activation, nationwide data infrastructure, and patient data contribution tools to reduce timelines, costs, and patient burden across clinical development.
|Articles|February 8, 2013
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 4-7 February 2013
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The European Medicines Agency’s
For an overview of all information available following the meeting of the PRAC, please see the table below.
The Agency publishes a new page following the PRAC meeting each month. The minutes of each PRAC meeting will be published during the week following the subsequent PRAC.
View the agenda and other sources
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