Webinar on International Evidence Requirements for Medical Devices

Stephen Hull, a 20 year veteran of medical device reimbursement will provide first hand insight into the core requirements of key global markets and offer advice on how to best assemble your global evidence strategy.

Detailed slide materials will provide the frameworks and pathways for reimbursement across the target markets. 
The session will also describe the latest developments in new requirements or hurdles posed in each market. 

Why should you Attend: 

Do you have global responsibility for a medical device product launch? This detailed review of country level frameworks and emerging requirements will give you a succinct landscape as well as understanding the emerging issues across the various markets that may change your product launch strategies. 

Areas Covered in the Session:

• Reimbursement agencies, pathways and requirements
• Evidence demands for new products
• Emerging requirements in the EU, Americas and Asia

• All global product managers
• Global Vice Presidents of Marketing
• All commercial leads with international responsibility

Speaker Profile: