Following the success of the first inaugural Congress in Prague, this second congress in conjunction with EAAR (European Association of Authorized Representatives) will address the important updates for Medical Devices. Topics to be covered, among others will be: � New Regulations strengthening the rules on placing medical devices on the market � Reinforcement surveillance � Manufacturers' responsibilities for the follow-up of the quality, performance and safety of their devices � The improvement trace-ability throughout the supply chain � The central database to provide patients, healthcare professionals and the public with comprehensive information on products available in the EU market � Authorized Representative vs the Qualified Person

Date : 16th October 2017 to 17th October 2017

Place : Germany, Berlin

Website :http://rmd2017.com/default.aspx

Contact Person:Rachel Katzir

Description:

Following the success of the first inaugural Congress in Prague, this second congress in conjunction with EAAR (European Association of Authorized Representatives) will address the important updates for Medical Devices. Topics to be covered, among others will be: • New Regulations strengthening the rules on placing medical devices on the market • Reinforcement surveillance • Manufacturers' responsibilities for the follow-up of the quality, performance and safety of their devices • The improvement trace-ability throughout the supply chain • The central database to provide patients, healthcare professionals and the public with comprehensive information on products available in the EU market • Authorized Representative vs the Qualified Person

Following the success of the first inaugural Congress in Prague, this second congress in conjunction with EAAR (European Association of Authorized Representatives) will address the important updates for Medical Devices. Topics to be covered, among others will be: � New Regulations strengthening the rules on placing medical devices on the market � Reinforcement surveillance � Manufacturers' responsibilities for the follow-up of the quality, performance and safety of their devices � The improvement trace-ability throughout the supply chain � The central database to provide patients, healthcare professionals and the public with comprehensive information on products available in the EU market � Authorized Representative vs the Qualified Person will be held in Berlin,Germany on date 2017-10-17

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Deadline for abstracts/proposals : 16th October 2017

Keynote Speakers :

Venue :Hilton Berlin, Mohrenstraße, Berlin, Germany

Check the event website for more details.