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Thursday, Jun 29, 2017 at 11:00 AM to 12:00 PM EST
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The release of MEDDEV 2.7.1 Rev 4 June 2016 on clinical evaluations in Europe led to the the principle challenges for device companies to ensure compliance to new requirements and making justification that the available data is sufficient to support the performance and safety of a device.Speaker:Dr. Frank TurnerGlobal Medical Director,Director of Medical AffairsSME National Institutes of HealthDate & Time: Thursday, 29th June 2017 , 11 AM -12 Noon EST | 5 PM - 6 PM CETClick here to register : https://www.makrocare.com/webinar-registration-for-device-compliance-with-meddev-2-7-1-rev-4-for-clin-eval-cer
https://www.makrocare.com/
MakroCare is a leading biotech, pharma and medical device consulting for Clinical Development, Regulatory affairs, Regulatory Operation, Publishing, Labeling, Med Affairs, Central Monitoring and RBM services.
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