top of page
.png)
.png)
ABOUT
​
This course is open to QA/RA professionals, consultants, and MedTech professionals, providing an opportunity to empower themselves across the MedTech industry with expert-led training and guidance on the European Medical Device Regulation (CE MDR) and In Vitro Diagnostic Regulation (IVDR). The course consists of 10 sessions, each designed to provide current and relevant insights into the CE MDR and IVDR developments. Every session is 1 hour, conducted via online, Zoom.
Upon full completion, participants will be awarded a certificate of achievement​
​
DETAIL
​
Date: April 2025 - January 2026
Venue: Online Platform (Zoom link TBC)
Session 1: 3 pm to 4 pm
Cost: Free for Session 1, €35/ SGD 53 per session from Session 2 onwards.
​
IMDS 2021 Course Programme
​
​
​
​
​
KEY BENEFITS​
-
Gain valuable insights and experiences from the key respected speakers in the field to apply to your work/decision and preventing common mistakes.
-
Gain a comprehensive understanding on global regulatory landscape and latest updates including the new CE MDR/IVDR enforcement.
CONTACT US
​
International Medical Device School (IMDS)
Managed by IMDS Group
​
ORGANIZERS
bottom of page