Medical Device Clinical Research & Reimbursement Conference

Understanding the Complex Nature of Conducting Medical Device Studies that Support Regulatory and Reimbursement Goals in a Cost and Time Effective Manner

January 11-12
Phoenix, Arizona

About the Conference

This conference program will bring together executives from industry to discuss and debate the challenges that they face in designing and conducting studies that support an increasing array of corporate goals. Keynote presentations will address topics of interest to clinical and reimbursement executives, on movements within the industry resulting in new evidence thresholds, as well as methods for bringing teams together throughout the product lifecycle to ensure targets are met.

Each afternoon, the audience will divide into break-out sessions that will focus more specifically on topics related to clinical research or reimbursement

Topics to Included

General Sessions

• Understanding the Impact of Changes in Health Policy on Evidence Requirements for Medical Devices
• Comparative Effectiveness Studies Impacting Medical Devices
• Understanding Coding Principles from the Clinical Research Perspective
  

 

And More...

 

Clinical Study Breakouts

• Optimizing Site Selection through working with Sales, Marketing and KOL’s
• Ethical and IRB Considerations in Subject Enrollment
• Understanding Pathways for Working with FDA to Secure Device Approval
• Opportunities in Post-Marketing Clinical Research

And more...

 

Reimbursement Breakouts

• Developing End points to Support Reimbursement in Post-Marketing Studies
• Preparing for and Understanding Health Technology Assessments
• Recognizing Differing Evidence Requirements for Private vs. Public Payers

And more...

 

Attendee Profile

Executives that will be most interested in participating in this conference program will be those involved in conducting global clinical research and securing reimbursement and market access for their new technologies. If you are involved in this process, or are considering developing a clinical study in the US or Europe, this conference is a must attend. Job titles of executives that will be most applicable for this program include VPs, Directors and Managers of:

• Clinical & Regulatory Affairs
• Clinical Operations, Clinical Research Associates
• Reimbursement & Market Access
• Health Economics & Outcomes Research
• Marketing and Business Development
• Chief Executive Officers & Chief Scientific Officers

To request the full conference agenda, registration details, and information on promotional pricing please contact:

Paul Hernandez, Marketing Manager
phernandez@Q1productions.com
312-602-9684