The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020

Topic : The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020

Register:https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1614&speakerid=269&SOURCE=EG_RD

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Overview

This webinar will discuss main differences between current EU Medical Device Directive (MDD) 93/42/EEC and new EU Medical Device Regulation (MDR) 2017-745 and how to ensure compliance with the new MDR requirements that will be mandatory starting 26-May-2020.

Areas Covered in the Session :

Device classification
Conformity routes
General Safety and Performance Requirements (GSPRs)
Technical documentation
Post market surveillance (PMS)
Clinical evaluation
UDI
EUDAMED
Economic operators

Speaker Profile :

Juan M. Campos is a keynote Speaker at Compliance Key. Juan M. Campos is a Medical Device professional with 32+ years of continued industry experience.His main areas of expertise include Quality Assurance, Regulatory Compliance and RegulatoryAffairs. He has led culturally and geographically diverse QA/RA teams in Spain, UK, France,Switzerland, Netherlands, Germany, Portugal, Italy, Greece and Turkey directly reporting to him.

Contact Info :

Compliancekey
https://www.compliancekey.us
Email : [email protected]
Phone :   +1 717-208-8666