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European Medical Devices Industry: An Impact Analysis of the Changing Regulatory and Health Economics Scenarios
GlobalData, Jan 2011, Pages: 8
European Medical Devices Industry: An Impact Analysis of the Changing Regulatory and Health Economics Scenarios
Summary
GlobalData’s report, “European Medical Devices Industry: An Impact Analysis of the Changing Regulatory and Health Economics Scenarios” provides key information and analysis on the regulatory and reimbursement environment for medical devices in the European market. The report provides information on regulatory and reimbursement changes ongoing or completed in the past two years in the Europe medical devices industry. It provides key insights and review of the changes and their impact on medical device firms and healthcare providers. All the key factors affecting the regulatory and reimbursement scenario has been analyzed with respect to the top five markets in Europe (EU5), which are Germany, France, the UK, Spain and Italy.
This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData’s team of industry experts.
Scope
- The 2007/47/EC Medical device directives and its impact.
- Trends in Health Technology Assessment Practices in Europe and its impact.
- Health Technology Assessment Practices in the EU5 countries.
- Trends in Diagnostic Related Groups (DRG) systems in Europe and their impact.
- Comparative Overview of DRG systems in EU5 countries.
- Austerity Measures in Europe and its impact.
Reasons to buy
- Develop business strategies by understanding the regulatory and pricing related trends and developments that are affecting the medical device market in Europe.
- Decide entry and market expansion strategies for the European medical equipment industry.
- Design and develop your marketing and sales strategies.
- Understand reimbursement scenarios in Europe and align efforts accordingly to achieve maximum reimbursement.
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