Free Webinar ”In Vitro Diagnostic Regulation 2017/746 (IVDR)”
Welcome to our free webinar, where we will give you the latest about the IVD Regulation, with date of application 26 May 2022. Are you already in compliance or are you working on the implementation?
During the presentation, we will go through the following:
IVDR requirements at a glance – what are the differences between requirements according to classification?
- Timelines – what shall already be in place?
- Transition timelines for the different risk classes
What is going on at the moment? Any news at …
- European commission?
- Swedish Medical Products Agency?
- Notified body?
- Swedish Labtech?
What to do with the RUO-marked devices, used in or together with your product?
Any new guidelines? Where do you find the news?
Webinar language: English
Date: 4 October, 08.30 – 09.30 incl. Q&AThe webinar will be administrated as a Zoom webinar.
Course Leader: Anna-Karin Areskog, Senior Quality and Regulatory Consultant
The event is free, but tickets are limited. Register now to participate.
If you have any questions or want to get in contact with us, use firstname.lastname@example.org.
- When: to
- Where: Online
- Organizer: QAdvis
- Language: English
Please register no later than Monday 2 October 2023