EMA.WGU.edu

Emer cooke, ema’s executive director: 2025 achievements in medicine regulation ema's executive director shares her end-of-year message and takes stock of ema's work in 2025. The medicine you are looking for may be authorised in individual member states via national procedures, rather than centrally via ema.

Only medicines evaluated by ema are available on. The european medicines agency (ema) plays a key role. Ema business hours over holiday period the european medicines agency's (ema) office is closed from 18:00 on 22 december to 08:30 on 5 january

The european medicines agency (ema) is responsible for the scientific evaluation of centralised marketing authorisation applications (maa). 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. Check ema's annual reports for insights into our regulatory procedures, activities, and achievements.

This complements information on medicines published on this website, which only includes medicines that the european medicines agency (ema) evaluates. 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.