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The european medicines agency is a decentralised agency of the european union responsible for the evaluation, supervision and safety monitoring of medicines. For more information on ema and its policy on the publication of clinical data, see the ema corporate website. Start your application today and open educational opportunities for your child.
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The ema was founded after more than seven years of negotiations among eu governments and replaced the committee for proprietary medicinal products and the committee for veterinary medicinal products, though both of these were reborn as the core scientific advisory committees. For more information on the clinical data on this website, see clinical data available The european medicines agency (ema) is a decentralised agency of the european union (eu)
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It is responsible for the scientific evaluation, supervision and safety monitoring of medicines.
The european medicines agency (ema) helps make sure that medicines used in the european union are safe, effective and of high quality Ema carefully evaluates medicines before they are approved and continues to monitor their safety once they are on the market. The european medicines agency (ema) protects and promotes human and animal health by evaluating and monitoring medicines within the european union (eu) and the european economic area (eea). 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. The mission of the european medicines agency (ema) is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the european union (eu). Ema is the first regulatory authority worldwide to provide such broad access to clinical data
