Webinar on International Evidence Requirements for Medical Devices

MessageThis Webinar is over
Date Mar 8, 2016
Time 10:00 am
Cost $150.00
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
Who Will Benefit:
  • All global product managers
  • Global Vice Presidents of Marketing
  • All commercial leads with international responsibility
Speaker Profile:
Stephen Hull has over 25 years of experience in health policy and medical product strategy, for medical devices, diagnostics, pharmaceuticals and biotech products. He is Principal and Founder of Hull Associates, a specialized global reimbursement strategy firm focused on medical device and diagnostic technologies. With 25 seasoned partners worldwide, his firm routinely assists in the development and execution of comprehensive strategies for product launch and reimbursement in major global markets. Prior to forming Hull Associates, he served as Sr. Vice President for Global Reimbursement at AdvaMed, in Washington, D.C., the leading U.S.-based medical technology trade association.

Contact Detail:

NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Email: support@compliance4All.com
Event Link : http://bit.ly/International_Evidence_Requirements_for_Medical_Devices


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