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



VenueMiddletown, USA - United States USA - United States

KeywordsMedicaldevice; Livewebinar; EU


Topics/Call fo Papers

Topic : The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020
Register :
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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
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 :
Email :
Phone : +1 717-208-8666

Last modified: 2020-04-09 15:55:23