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8 october 2025, 10:00 (cest) Data on this website this website contains clinical data published under the european medicines agency (ema) policy on the publication of clinical data. Evaluation, supervision and safety monitoring of medicines in the eu.

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Search ema's news announcementsparacetamol medicines can be used in pregnancy, in accordance with official recommendations The european medicines agency (ema) publishes detailed information on the medicines assessed by the committee for medicinal products for human use (chmp) and committee for medicinal products for veterinary use (cvmp). The purpose of the european medicines agency's (ema) certification scheme for human and veterinary medicines is to confirm the medicine's marketing authorisation status and that it complies with good manufacturing practice (gmp) standards.

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.

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.