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

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


Online registration is available until: 7/30/2019
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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.

 

All registered attendees will receive an email the morning of the webinar with log in details.

You must be logged in to register.  If you have any questions or need assistance, please contact Sheri at sdevinney@medicaldevices.org.