MDMA Member Only Webinar: Europe's MDR & Proposed Pan European HTA Process for Reimbursement
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MDMA Member Only Webinar: Europe's MDR & Proposed Pan European HTA Process for Reimbursement

7/30/2019
When: July 30, 2019
2pm - 3pm ET
Where: United States
Contact: Sheri DeVinney
202-354-7171


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MDMA Members can view an archived recording of this webinar by CLICKING HERE.

 
On July 30th, MDMA will present a (no cost) member-only webinar, Europe's MDR & Proposed Pan European HTA Process for Reimbursement, hosted by Stephen Hull, Hull Associates.
 
While evidence requirements have changed under the new European framework for CE marking, the movement towards pan-European Health Technology Assessment also has gained traction, prompting greater conformity of HTA evidence requirements and "transplantation" of evidence reviews across geographies within the European Union.  Companies can expect CE mark requirements to be more aligned with the demands of HTA bodies for reimbursement, but the challenges for medical device firms are greater, as local HTA bodies may be commissioned to implement assessments that have a pan-European impact.