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Evaluation, supervision and safety monitoring of medicines in the eu. Some of the information in these systems is available to all visitors, such as details about clinical trials in the eu, reports of. 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. Ema has several websites and systems to support its work Follow the journey of a medicine for human use assessed by ema in this interactive timeline
It explains all stages from initial research to patient access, including how ema supports.
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. 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. 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.
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