Register for the GUIDE.MRD Webinar on
Notified Bodies’ Roles and Perspectives on IVDR Clinical Performance Studies
Session Description:
Bringing an innovative diagnostic assay to market is an exciting yet complex journey. Compliance with the In Vitro Diagnostics Regulation (IVDR) is one of the key steps to ensure the safety, performance, and reliability of IVDs. What role do Notified Bodies play in this process, and what are their needs and expectations?
Join us for an insightful webinar, during which representatives from Notified Bodies will illuminate their critical role in ensuring compliance with IVDR and navigating evolving regulatory landscapes. Whether you are a patient who could benefit from more targeted treatments, a healthcare professional involved in treatment decision-making, or part of the regulatory and market adoption process, this session will provide key insights to help you understand the regulatory landscape and path to adoption.
Open to all stakeholders, from GUIDE.MRD partners to regulators from:
🗓 21 May 2025
🕒 3 PM CEST / 10 AM ET
Please click the following link to register: Registration Form
