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Market Research Reports in Medical Devices |
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ADI Medical Innovation in Healthcare |
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Healthcare Systems and Reimbursement for Medical Devices in Europe
A valuable report for anyone involved in Medical Device marketing in Europe |
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Whilst Europe is a single market and efforts are constantly being proposed and legislated to bring the community closer together, there remain fundamental differences within the member states, not least in the disparity of structure in their healthcare systems. It is the case however that of the $72bn market in 2010, almost 80% is accounted for within the major markets of Germany, UK, France, Italy and Spain. Although with the addition of new markets to the European union, this balance is beginning to shift. |
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What’s more, in the 2010 climate, these differences are not going to change or see any significant “coming together”, with the only likelihood in the foreseeable future being ever more downward pressure on health expenditures. On the Regulatory front a recent amendment to the Medical Devices Directive has come into force in 2010 (Directive 93/42/EEC) and whilst many parts of this involve clarification, there are some fundamental changes that manufacturers and suppliers need to be aware of in order to ensure future or ongoing compliance with European law. |
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Compliance is a critical aspect of course however once attained, companies need to understand the differing systems of Healthcare provision in each European market, in order to be able to exact effective marketing strategies. This report therefore examines these differing structures in the states of the European Union, with particular emphasis on the major markets. Assessment of the requirements for the local marketing of Medical Devices and the systems and protocols for reimbursement, where relevant are also fully analysed. The complexities and differences in the individual country systems make this report an essential guide to anyone marketing, or intending to market Medical Devices in Europe. |
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Report Contents:
· Introduction · EC Medical Devices Directive (93/42/EEC), CE Marking - Overview, including analysis of requirements of Directive 93/42/EEC, implemented in 2010 · Healthcare Provision and Systems in Europe, Country Commentary 2011 · Germany, France, UK, Italy, Spain, Ireland, Scandinavia, Benelux, Austria · Other EU Member States · Norway, Switzerland · Reimbursement Systems 2011 · Country scenarios, as above · Opportunities, Summary, Conclusions |
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