Support to research

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The European Medicines Agency plays an important role in the innovation and availability of medicines for human and veterinary use through its support to research activities within the European Union (EU) and beyond. In its role in the EU’s regulation of medicines, the Agency is in a unique position to contribute to scientific debate by providing experience and expertise in areas related to medicine development and medicine safety.

The Agency works across a wide number of topics and with a broad range of stakeholders, from research institutes, universities and public-private initiatives to the European Commission and EU Member States. Activities range from acting as the secretariat for multipartner networks to membership of pan-European and international research projects.

All of the Agency’s work aims to improve the science and process of medicines regulation to foster the development of medicines for unmet medical needs, and to optimise the surveillance and management of medicines on the EU market.

The Agency’s road map to 2015 and work programmes underpin the Agency’s activities in this area, as part of its mission to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health. As part of this aim, it is important for the Agency to be aware of the latest scientific knowledge and methodologies and to actively support science in relevant areas.

The Agency also supports the overarching aims of the EU framework programme for research and innovation.

Involvement of the Agency in research activities

The Agency has targeted engagement with academia, learned societies and research groups in a range of areas, where they enable the Agency to move forward in its mission. These areas include:

A list of the current research projects that Agency is participating in is available under research projects.

Working with the Agency

The Agency may be able to take part in certain research projects in collaboration with external parties, if the projects support the Agency’s health mission. The Agency can take part on a number of levels:

  • as coordinator of a research project;
  • as a participant in research activities;
  • with an advisory role.

The Agency bases its decisions on which projects it can take part in on these criteria:

  • the applicability and relevance to the Agency’s work;
  • the added value of contribution from regulators to the project;
  • the need for continuing and strengthening collaboration with other institutional and international bodies;
  • the quality and soundness of the research proposal;
  • confidentiality and access to data;
  • conflicts of interest.

The Agency welcomes the sharing of results and data with potential public-health impact by researchers, even before these have been published in a peer-reviewed journal.

Full details of the types of activities that the Agency is involved in, the degree of involvement, funding arrangements and the process for enquiring about embarking upon a research project with the Agency are available in this document:

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