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Find information on centrally authorised medicines Ema evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients. Find all new and updated information published on our website in one place
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Find answers to the most frequent asked questions we receive For more information on ema and its policy on the publication of. 13 new medicines recommended for approval
Another 8 medicines recommended for extension of their therapeutic indications.
Log in to your provider account at step up for students to manage services and payments, ensuring seamless support for educational programs. Start your application today and open educational opportunities for your child. The european medicines agency (ema) is an agency of the european union (eu) in charge of the evaluation and supervision of pharmaceutical products Prior to 2004, it was known as the european agency for the evaluation of medicinal products (eaemp) or european medicines evaluation agency (emea)
[4][5] the ema was set up in 1995, with funding from the. The european medicines agency (ema) is a decentralised agency of the european union (eu) It is responsible for the scientific evaluation, supervision and safety monitoring of medicines. 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).
Evaluation, supervision and safety monitoring of medicines 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. Ema is the first regulatory authority worldwide to provide such broad access to clinical data For more information on the clinical data on this website, see clinical data available
