REGISTRATION IS OPEN FOR THE INTERNATIONAL MEDICAL DEVICE REGULATORS FORUM

https://www.imdrf.org/?utm_medium=email&utm_source=govdelivery The FDA, as the Chair and Secretariat of the International Medical Device Regulators Forum (IMDRF) in 2024, is hosting the 25th session of the IMDRF in Washington, D.C., the week of March 11. We cordially invite you to participate in the IMDRF’s public meeting on March 11-12 when regulators, industry, academia and other key stakeholders from across the international medical device community will come together to exchange information, generate ideas and hear updates on IMDRF’s various working groups as they strive to accelerate international medical device regulatory harmonization and convergence. Global Medical Technology Alliance (GMTA) http://www.globalmedicaltechnologyalliance.org/index.html?utm_medium=email&utm_source=govdelivery Day One of the meeting is a joint workshop with the Global Medical Technology Alliance – national and regional medical technology associations – and the Global Diagnostic Imaging, Healthcare ICT, and Radiation Therapy Trade Association or DITTA. Day Two will be an IMDRF Stakeholder Open Forum. The meeting will be held at the Ronald Reagan Building and International Trade Center at 1300 Pennsylvania Avenue NW, Washington, D.C. Although we highly encourage your participation in person, a virtual option to livestream the meeting will be available. Registration closes on February 16, 2024. To secure your spot, please register at https://events.espinc-usa.com/imdrf032024/begin. https://events.espinc-usa.com/imdrf032024/begin?utm_medium=email&utm_source=govdelivery If you have any questions, please contact the Secretariat at IMDRF2024@fda.hhs.gov.