2020 - Your EU MDR Journey Continues: An Insight Into Strategic Approaches For Collecting Clinical Evidence In The Post-Market Era
Date2020-08-28
Deadline2020-08-27
VenueOnline, Canada
KeywordsClinical Operations; Clinical Development; European Medical Device Regula
Topics/Call fo Papers
This webinar is part of a series. Whereas the main focus of the previous webinar (August 4) referred to the premarket phase, this webinar will have a post-market focus. Both webinars can be attended separately, and knowledge of the other webinar is not required. However, as Aristotle already pointed out, the whole is greater than the sum of its parts! Attendance of both webinars will provide you the full journey throughout the clinical lifetime of the device.
Other CFPs
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- How Patient Assistance Programs (PAPs) are Being Modernized with Innovative Technologies
- Are You Protecting Employees During HPAPI Manufacturing?
Last modified: 2020-08-13 23:03:32