From MDD to EU MDR

Conducted by: Mr. Robert Van Boxtel
Print version

Share a colleague:

Dates: 
  • 11/11/2019
  • 13/11/2019

מתעניינים? לחצו כאן

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

    Course price: €1,048 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
    תחזוקת מערכת האיכות בזמן מלחמה QMS

    Leave a Reply



      [anr_nocaptcha g-recaptcha-response]