May 27, 2025 10:30 – 11:15 CET
Join our Free Webinar on IVDR Compliance for In Vitro Diagnostic Medical Device Manufacturers
With the upcoming IVDR compliance deadline at the end of May, it’s crucial to ensure your organization is fully prepared. This webinar will provide a comprehensive overview of the most critical aspects of IVDR compliance, including regulatory requirements on the quality management systems, and product lifecycle planning.
Our expert-led session will draw on content from our specialized courses, offering you valuable insights and practical guidance to navigate the complexities of IVDR requirements, including how IVDR implementation is supported by ISO13485:2016, as well as the requirements that your quality management system must address that is not covered by that standard.
Don’t miss this opportunity to gain insights on how your compliance strategy can ensure your products meet the new requirements.
Note. 26 May 2025 is the deadline to have an IVDR QMS in place.
