From lab to patient: journey of a medicine

Published by EMA

Regulatory Affairs Marketing Authorisation EU Marketing Authorisation Road Map EMA Drug Development Scientific Advice Committee for Orphan Medicinal Products Centralised Procedure National Procedure

Follow the journey of a medicine for human use assessed by EMA in this interactive timeline. It explains all stages from initial research to patient access, including how EMA supports medicine development, assesses the benefits and risks and monitors the Safety of medicines.

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