Getting your Trinity Audio player ready...
|
Table of Contents
This is your event if you want to discover the solution covering all MDR requirements!
Medical Devices Regulation (MDR) has been fully applicable since the mid of 2021, and every medical device manufacturer have to face new challenges >>
Traceability of Medical Devices: The solution to the challenges was the natural extension of the previous webinar when we looked in-depth into the MDR and new requirements. Now, we will go straight to the solution of all challenges in front of supply chain participants. The webinar will discover how to meet the requirements and benefit from them.
Event details:
Date: 2 February 2022
Working language: English
What did you learn about:
Short MDR resumeย โ regulation, classification, timeline
Our experience till the momentย โ approach and expertise; examples; cases
Our solutionsย โ different types of solutions to the specific cases
What`s next?ย โ EUDAMED modules, tendencies in medical devices serialization
Q&A session
Speakers:
Mihail Ivanov – Sales Development Representative @SoftGroupย
Maria Docheva – Marketing Specialist @SoftGroup
Go to Webinar`s Recordingย >>
The video is available on-demand HERE.