Medical Device Regulatory Clearance & Approval Conference: Attendee Profile

Executives that will be most interested in participating in this conference program will be those involved in securing regulatory approval for new and existing medical devices. Understanding how to navigate the regulatory landscape is a challenging process, and our panel of expert presenters have over 200 years of combined experience introducing new products into the market. If you are involved in this process, or are considering the various FDA regulatory approval routes for a new device, this conference is ideal. Job titles of executives that will be most applicable for this program include Vice Presidents, Directors and Managers of:

• Regulatory Affairs
  
• Worldwide Regulatory Affairs
  
• Regulatory Specialist
  
• Quality & Regulatory
  
• Quality Assurance
  
• Corporate Regulatory Affairs
  
• Clinical Affairs
  
• Regulatory Submissions