DNV GL Singapore

MDR annexes Webinar

Learn more on MDR Annexes to get you prepared for the Medical Device Industry

Event Information

MDR (Medical Device Regulation) annexes

The MDR regulation will replace the current Medical Device Directive (MDD) and the active implantable Medical Device Directive (AIMD). MDR is including 17 annexes.

In this webinar series, we will focus on Annexes of MDR

The webinar will cover:

  • Introduction of MDR and annexes
  • MDR vs. MDD: Key changes in Annexes
  • How to prepare your organisation for the changes

Plus, this webinar will help you be familiar with MDR annexes and consider what actions you need to start now to be prepared for the changes in the MDR and providing Technical Documentation. 

Missed out our first series? Find out more on MDR and CE Marking Webinar here!

Our Presenter

Hasan Zarin Mehr is Lead Auditor/MDD Assessor at DNV GL with nearly 12 years’ experience in Medical Device Industry, who previously worked as a Medical Device Technical Specialist, QMR/QA/RA and has worked in consulting & Training to vast range of Medical Device manufacturers for implementing Quality Management System in accordance with ISO 13485 and Providing Technical Documentation for CE Certification in all classes of Is, Im, IIa, IIb and III.
His qualifications include a MSc in Biomedical/Biomaterial Engineering and a BSc in Biomedical Engineering.