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The European Medicines Agency (EMA) publishes a full work programme and annual report, to provide an overview of the work of the Agency together with the European medicines regulatory network.

The European Medicines Agency (EMA) has been interacting with European healthcare professionals in various areas of its work since it was founded in 1995.

The European Medicines Agency (EMA) and patients have been actively interacting since the creation of the Agency in 1995. This cooperation was extended to include consumer groups with an interest in medicines.

The European Medicines Agency has advisory functions and support services that support the Executive Director and the Agency on a range of operational, policy and scientific issues in their various fields of expertise.

The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.

The European Medicines Agency (EMA) engages with a network of eligible patients and consumers organisations, ensuring that their needs and concerns are represented via direct contact with the Agency.