Introducing Medical Device Regulation (MDR) Training Course

Understand the requirements of MDR

LIVE VIRTUAL TRAINING SCHEDULE

Introducing Medical Device Regulation (MDR) Training (9 am to 6 pm SGT | 1 Day)

  • 31st March 2021
  • 31st May 2021

WHAT YOU'LL GAIN BY ENROLLING FOR THIS COURSE?

  • Get an understanding of MDR
  • Gain insights on the changes for European Union’s Medical Devices Regulation (MDR 2017/745/EU)
  • Learn about MDR requirements 
  • A globally recognized course completion certificate

ABOUT MDR TRAINING COURSE

This comprehensive course will provide participants with an introduction to MDR, the classification of medical devices and conformity assessment procedure. Participants will get an in-depth understanding of the MDR requirements including:

• Technical documentation requirement
• General Safety and Performance Requirements
• Clinical data & clinical evaluation requirements
• Post-Market Surveillance, vigilance and market surveillance requirements

TRAINING DURATION

1 Day Instructor-led training

WHO SHOULD ATTEND?

This course is suitable for Medical Device professionals (that are in areas such as Quality & Risk Management, R&D, Manufacturing etc.) and anyone who is working in the Medical Device sector that market products to the EU.

LEARNING & CAREER BENEFITS

  • Get a good understanding of MDR
  • Equip you with knowledge on your organisation can meet the requirements of the MDR

PRE-REQUISITES

None.

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