The IVD industry is about to change
Discuss the impacts of the IVDR with the MHRA and key Notified Bodies, and hear how industry is making the move to the IVDR.
Delve into the details of the IVDR
- Implementing the IVDR – Competent Authority, Notified Body and industry perspectives
- Understanding the implications of the new clinical evidence requirements
- Do you understand the responsibilities of the Person Responsible for Regulatory Compliance?
- How will PMS and vigilance requirements change under the IVDR?
- What challenges is the IVDR creating for companion diagnostics manufacturers?
Competent Authority and Notified Body perspectives from:
Join the discussion
Our interactive sessions will allow you to:
- Discuss how to implement the IVDR with the MHRA, LRQA, UL, and industry
- Share experiences with increased clinical data requirements
- Understand how the companion diagnostics industry should be preparing for the IVDR