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Only medicines evaluated by ema are available on this website You may not be able to obtain a complete list of available treatment options for a specific condition by searching on ema's website. 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.
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). On this page you can find several ways to contact the european medicines agency (ema) depending on your need for assistance or type of request. In 2024, ema recommended 114 medicines for marketing authorisation Of these, 46 had a new active substance which had never been authorised in the european union (eu) before.
The european medicines agency (ema) provides scientific and regulatory guidance to pharmaceutical companies whose medicinal products have been authorised in europe In the european union (eu) they must undergo a conformity assessment to demonstrate they meet legal requirements to ensure they are safe and perform as intended They are regulated at eu member state level, but the european medicines agency (ema) is involved in the regulatory process.
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