From MDD to EU MDR

Conducted by: Mr. Robert Van Boxtel
Print version

Share a colleague:

  • 11/11/2019
  • 13/11/2019
Course location: Kfar Maccabiah, Ramat Gan
Duration: 1-Day Course
Hours: 09:00 - 17:00
Credits: 2
Course Language: English

Course price: $1,184 Including VAT
Early registration is Closed
Do you have a subscription? You deserve more

Have a question? We got all the answers

Issues to be covered

Day 1:

  • Introduction, including timelines
  • Scope of the MDR (Article 1), new/revised important definitions (Article 2) and Eudamed
  • Economic Operators – their roles, rights and responsibilities
  • Impact for Health Institutes in the EU + Custom made devices

Day 2:

  • Classification and Conformity Assessment routes
  • QMS requirements – including comparison to ISO 13485:2016
  • Annex I: General Safety and Performance Requirements
  • Annex II: Technical Documentation requirements
  • Post Market Surveillance, including vigilance, FSCA.

Who should attend

This course will be extremely useful for the persons working in regulatory and quality assurance departments, and equally important for project managers or CTO’s involved in development of new medical devices. Last but not least, as CEO of a medical device company, you will obtain a clear insight in the new EU requirements and the impact it will have on your business case or company.

Benefits to the Participants

At the end of the seminar, you will be able to draft your company’s action plan, enabling working towards EU MDR compliance throughout the lifecycle of a medical device.

About The Lecturer

Robert Van Boxtel
Robert van Boxtel has over 20 years of experience in
Read more

Leave a Reply

    [anr_nocaptcha g-recaptcha-response]