Business Profile
European Medicines Agency (EMA) provides evaluation, supervision, and safety monitoring of medicines for the European Union.
Healthcare professionals, pharmaceutical industry stakeholders, patients and consumers, animal health professionals, and academia.
EMA is a decentralised agency of the European Union, ensuring medicines' safety and efficacy within the EU through centralised evaluation and supervision.
Ongoing evaluation and updates; specific timelines depend on individual medicine evaluations and authorisation processes.
The EMA is responsible for the evaluation, supervision, and safety monitoring of medicines within the EU.
The European Union, specifically healthcare professionals, patients, pharmaceutical companies, and veterinary medicine stakeholders.
EMA provides centralised regulatory oversight across the EU, ensuring medicines' safety and efficacy and facilitating access to new therapeutic solutions.
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