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EMEA Roadmap 2010 The European Medicines Agency (EMEA) initiated an external consultation exercise with the publication of The European Medicines Agency Road Map to 2010. The Road Map provides the EMEA viewpoint on how it should prepare for the challenge that the European Union regulatory system will face in the future. It puts forward the EMEA's vision on its contribution, the objectives that need to be achieved and what prerequisites need to be fulfilled. Stakeholders were invited to comment on the Road Map. EVM's Comments on the Road Map highlight the unique characteristics of vaccines and put forward a number of points for consideration. © European Vaccine Manufacturers (EVM) - a specialised group of EFPIA 2007 |
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