Ms. Ajda Mihelčič
Deputy Manager
Publishing Department
Ms. Ajda Mihelčič
Deputy Manager
Publishing Department
SPEAKERS
SPEAKERS
Mr. Roland Gerald
RA Manager
Quality Management System Department
Mr. Roland Gerald
RA Manager
Quality Management System Department
Ms. Helene Quie
Managing Director
Qmed Consulting Co.
Ms. Helene Quie
Managing Director
Qmed Consulting Co.
WHEN
Wednesday, 8th July
from 15:00 to 16:00 CET
WHEN
Wednesday, 8th July
from 15:00 to 16:00 CET
JOIN THE WEBINAR!
JOIN THE WEBINAR!
CONNECTION
You can connect from your computer or mobile device.
You will receive all the details by e-mail
CONNECTION
You can connect from your computer or mobile device.
You will receive all the details by e-mail
MDR DELAY WEBINAR
MDR DELAY WEBINAR
0
0
€
€
All Right Reserved 2020 © Obelis Group
All Right Reserved 2020 © Obelis Group
Stay in touch
Stay in touch
Interested in other webinars? Let us know!
Interested in other webinars? Let us know!
Complying with the EU Market Regulations can be a daunting task to undertake on your own. Make sure you get all the information you need.
We bring our experience and knowledge in the medical devices and in-vitro diagnostics industries, so don't miss the webinar!
Complying with the EU Market Regulations can be a daunting task to undertake on your own. Make sure you get all the information you need.
We bring our experience and knowledge in the medical devices and in-vitro diagnostics industries, so don't miss the webinar!
31 YEARS OF QUALITY
SERVICE IN REGULATORY AFFAIRS
31 YEARS OF QUALITY
SERVICE IN REGULATORY AFFAIRS
WE WILL BE COVERING:
WE WILL BE COVERING:
MDR Delay Explained
MDR Delay Explained
THERE ARE AT LEAST 5 THINGS YOU THINK YOU KNOW ABOUT THE MDR...
THERE ARE AT LEAST 5 THINGS YOU THINK YOU KNOW ABOUT THE MDR...
08 July, 16:00 CET
Save the Date!
08 July, 16:00 CET
Save the Date!
Vigilance & Incident Reporting
Vigilance & Incident Reporting
Clinical Evaluation Report
Clinical Evaluation Report
MDR Delay: What has changed?
MDR Delay: What has changed?
Remember, the 1-year delay will provide you with additional time to finalize your compliance with the MDR, which is a complex and lengthy process!
But what does this entail for Medical Device manufacturers?
Join the FREE MDR Webinar to find out and hear the latest changes from the regulatory experts! We will be covering:
- MDR delay explained
- Vigilance & Incident Reporting after DoA
- Clinical Evaluation Report based on the MDR
Remember, the 1-year delay will provide you with additional time to finalize your compliance with the MDR, which is a complex and lengthy process!
But what does this entail for Medical Device manufacturers?
Join the FREE MDR Webinar to find out and hear the latest changes from the regulatory experts! We will be covering:
- MDR delay explained
- Vigilance & Incident Reporting after DoA
- Clinical Evaluation Report based on the MDR
