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Information on medicines and related procedures includes a reference to relevant substances

Inn or common name, active substance, and english common name for.

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) is responsible for the scientific evaluation of centralised marketing authorisation applications (maa) Once granted by the european commission, the centralised marketing authorisation is valid in all european union (eu) member states, iceland, norway and liechtenstein.

Questions and answers about ctis and the clinical trials regulation ema's query management working group prepared a document to address the main questions received from sponsor associations about ctis and the clinical trials regulation Ema published this document in february 2023. The european medicines agency (ema) coordinates the european union (eu) pharmacovigilance system and operates services and processes to support pharmacovigilance in the eu. Ema concludes its two mandates as chair icmra elects new chair in amsterdam