Medical Device Reimbursement Integration
A Better Approach for Commercial Success

Tuesday, Nov. 7, 2017 · 1:30 p.m. - 3:00 p.m. EST

Devicemakers often take a step approach to commercialization: you develop your medical device, get it approved, and then determine a reimbursement policy. That’s not best practice any more.

A better way is to start early, developing your device with reimbursement considerations from the moment you start planning. There’s a name for it — “reimbursement integration.” This webinar will tell you how to execute it ... and avoid the many pitfalls of the step approach.

Presenter Tim Hunter has 20 years’ experience analyzing new and emerging technologies to get the most out of FDA submission and approval processes. When you sign up, prepare to discover: 

  • Simple — but effective — ways to integrate reimbursement planning early without spending a dime more — and maybe many dimes less — than you do right now

  • How to turn FDA-required data into an argument for health economics

  • How your FDA negotiations will impact your market

  • How to evaluate reimbursement needs vs. regulatory or clinical requirements

  • And much more!

No point wasting money on outmoded reimbursement techniques. Cut those costs — and maybe even get greater reimbursement — by integrating reimbursement at the start of the new-device process. Register now.

 

Who Will Benefit

  • CEO/CFO/COO
  • Reimbursement Managers
  • Marketing Managers
  • Regulatory Managers
  • Clinical Managers

 

Webinar plus Audio Recording/Transcript
Learn more

$487

add to cart

Webinar only
Learn more

$287

add to cart

24/7 Encore plus Audio Recording/Transcript
Learn more

$487

add to cart

24/7 Encore Presentation
Learn more

$287

add to cart

Audio Recording/Transcript
Learn more

$287

add to cart

 

 

 

Meet Your Presenter

Tim Hunter

Vice President
Musculoskeletal Clinical Regulatory Advisers, LLC

Tim Hunter has 20 years of experience analyzing new and emerging technologies from a reimbursement perspective. He incorporates an understanding of FDA submission and approval processes, and clinical trial development and management, to design reimbursement strategies that maximize collection of meaningful evidence within clients’ budgets.

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.

Phone (703) 538-7600 | Fax (703) 538-7676 | Toll free (888) 838-5578 | Email customerservice@fdanews.com

© 2017 FDAnews