WHAT IS IT ALL ABOUT ?
IZiel is pleased to invite you for the webinar on the EU-MDR Transition to meet the EU MDR 2017/745 requirements. Do not miss this opportunity, to learn about stringent MDR requirements for QMS, Technical Documentation, Economic Operators and UDI System.
Comprehensive
Detailed list of activities to be completed
Relevent
Class I, II & III medical device manufacturers
Customer Focused
Understand importance of time & budget
SPEAKERS AND TOPICS
Atul Mahajan
Director – Engineering Services
Abhishek Mishra
Director – Centre of Excellence
Topics Covered
- Overview of QMS requirements and Technical Documentation Structure
- Major changes required in Technical Documentation as per MDR requirements
- Changes in Device Classification Rules
- Requirements for Economic Operators
- Implementation of UDI System
- Overview of General Safety and Performance Requirements
- Overview of PMS and Vigilance requirements
GALLERY
Preview of the Seminar conducted by IZiel along with their partners.
This Webinar is conducted by IZiel