Introduction into the EU IVDR 2017/746 - the new EU regulation for invitro diagnostic medical devices training seminars presented by ComplianceOnline register now on FindaSeminar.com

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Introduction into the EU IVDR 2017/746 - the new EU regulation for invitro diagnostic medical devices  

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For:

CEO’s of companies, which sell in vitro diagnostic medical devices to Europe, Regulatory Affairs Managers of companies, which sell in vitro diagnostic medical devices to Europe, Quality Managers of companies, which sell in vitro diagnostic medical devices to Europe,Quality Representatives of companies, which sell in vitro diagnostic medical devices to Europe,Other managers, which need to deal with regulatory or quality guidelines

Cost:   

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Seminar Summary:

This course will give an introduction into the new in vitro diagnostic medical devices regulation EU IVDR 2017/746 in the European Union. (see full course description)

 

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Training Course Syllabus:


Learning Objectives:



  • What are the requirements of the new EU IVDR 2017/746?

  • Which Companies must apply the new EU IVDR 2017/746?

  • How to implement the new EU IVDR 2017/746 in a smart way into a medical device quality management system and how to apply the new regulation on your products to receive a new product certificate until May 2022?

  • How work the EU IVDR 2017/746 product reviews?

  • How work the EU IVDR 2017/745 quality management audits?


Seminar Summary:

This course will give an introduction into the new in vitro diagnostic medical devices regulation EU IVDR 2017/746 in the European Union. (see full course description)

print this agenda print agenda for the Introduction into the EU IVDR 2017/746 - the new EU regulation for invitro diagnostic medical devices training seminar

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