Webinar on Growing need of Clinical Data, PMCF & Registries for Devices
MakroCare is organizing the webinar on Growing need of Clinical Data, PMCF & Registries for Devices.
- (1888PressRelease) October 18, 2017 - This webinar will review emerging PMCF, Registry needs in this era of pre-MDR business risk evaluations.
Post Market Clinical Follow Up (PMCF) studies are a critical component of the clinical evidence required to comply with the new European regulations. As Clinical Evidence Reports (CERs) encounter more and more scrutiny by Notified Bodies (NBs), the gaps surrounding past PMCF work are becoming more evident. "Passive" collection of adverse events, complaints and the like may not be sufficient any longer to demonstrate conformity to the Essential Requirements and to the future Medical Device Regulation (MDR).
Speaker:
Dr. Joy Frestedt
Regulatory & Clinical Expert, Medical Device
Date & Time: Wednesday, Nov 15, 2017 , 11 AM - 12 Noon EST | 4 PM - 5 PM CET
Register here : https://www.makrocare.com/webinar-registration-growing-need-of-clinical-data-pmcf-registries-for-devices
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