Medical Devices Summit Europe

 Join us for two days of panels, presentations and networking opportunities with high-level individuals from across the industry as we discuss the hottest issues, including:

• Regulatory updates and changes to the 510(k) and the EU Directive
• Strategies for successful submissions, maintaining compliance and improving quality
• Spotlight presentations on foreign markets, including: 
o Expanding into foreign markets
o Integrating best practices into your clinical trials
o How reimbursement varies in different markets
o Usability and device design
o Best practices for international recalls