An interview with Sarah You about her experience in following one of our expert’s professional trainings on EU Regulations and the insights she gained from it.
Webinars and events
Webinar: EUDAMED Actor & Device registration
Register and learn all the details about EUDAMED, the European database for medical devices and In-vitro diagnostics!!
Seminar: Placing Medical Devices and In-Vitro Diagnostic Devices on the Union Market (EU) – News and Challenges
Register for our new live webinar about MDR and IVDR! On December 19, at 3:00 pm (Beijing Time), in collaboration with TÜV SÜD and AKRA TEAM GmbH!
Obelis group awarded as Great Place to Work 2022!
Investing in our employees is of paramount importance to us. We are more than honored to be awarded as Great Place to Work 2022!
Webinar: EU- UK GDPR Requirements & Implementation
Discover the new GDPR obligations for businesses and organizations within the EU and UK!
Webinar: Recent EU Regulatory Changes
Discover the latest EU Regulatory changes with our consultant Francesca Santacatterina!
Webinar: IVDR vs IvDO
Join our latest Webinar about the EU IVDR vs. the Swiss IVDO.
Watch the recording to discover all the details from our expert!
Flash 15 minutes webinar: Responsible Person and Safety Assessor
In this webinar, we will give answers to the most frequently asked questions from our cosmetic manufacturer clients!
Register and get the recording now!
EU IVDR now applies in Europe:What should IVD manufacturers do to comply?
If you are unsure of how you should now proceed in order to import new devices or maintain the previous ones in the European territory, this webinar is what you were looking for! Register now!
IVDR Webinar: Complying with the IVDR Legacy Requirements
Join our latest Webinar about IVDR. Davide Turchi, Manager of the Regulatory Affairs department at Obelis Group, will walk you through all the challenges related to Legacy Requirements!