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Evaluation, supervision and safety monitoring of medicines in the eu. While the majority of new, innovative medicines are evaluated by ema and authorised by the european commission in order to be marketed in the eu, most generic medicines and medicines available without a prescription are assessed and authorised at national level in the eu. Check ema's annual reports for insights into our regulatory procedures, activities, and achievements
The reports include an interactive timeline and figures and statistics for easy comprehension. Ema closed on 15 august for assumption day the european medicines agency's (ema) office is closed from 18:00 on 14 august 2025 to 08:30 on 18 august 2025 Information on the regulation of medicines for human use in the european union (eu), with a focus on the centralised procedure
The european medicines agency (ema) plays a key role in this 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. Data on this website this website contains clinical data published under the european medicines agency (ema) policy on the publication of clinical data.
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