Register and learn all the details about EUDAMED, the European database for medical devices and In-vitro diagnostics!!
Webinars
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!
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!
Webinar: Clinical Investigations
In this webinar, our top experts suggest strategies and best practices.
Obelis Roundtable on IVDR: How to get ready?
While every In Vitro Diagnostics brand journey, mission and merchandise are different, the regulatory compliance…