The European Medicines Agency (EMA) has launched a public consultation on its Road Map to 2015, which outlines its priorities for the next five years and continues its previous five-year Road Map initiative.
European and international partners, stakeholders, including patients' and doctors' organisations as well as the pharmaceutical industry, and the public are invited to make their views known on the document, entitled The European Medicines Agency Road Map to 2015: The Agency's contribution to Science, Medicines, Health.
Building on the achievements of the previous Road Map initiative, covering 2005 to 2010, the focus of the new Road Map is on continuous high-quality delivery of the Agency's core business in an increasingly complex regulatory and scientific environment.
Comments should be sent using the Agency's comments form by April 30, 2010 to: roadmap@ema.europa.eu
Final adoption is expected to take place in December 2010.
No results were found
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