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The U.S. Food and Drug Administration (FDA), as the Chair and Secretariat of the International Medical Device Regulators Forum (IMDRF), will host the 25th Session of the IMDRF in Washington, D.C., on March 11-15, 2024. Medical device stakeholders — including regulators, industry, academia, and the media — are invited to attend a free event that is open to the public, virtually or in-person, on March 11-12. The last three days (March 13-15) are for IMDRF invitees only.
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When: March 11-12, 2024 (Open to the public. To attend, please register below)
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What attendees can expect: Stakeholders from across the international medical device community will 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. Check out the agenda:
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Day One: IMDRF Joint Workshop with the Global Medical Technology Alliance and the Global Diagnostic Imaging, Healthcare ICT, and Radiation Therapy Trade Association (DITTA) on Medical Device Regulatory Reliance
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Day Two: IMDRF Stakeholder Open Forum
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Attend in-person or virtually: The event will be held at the Ronald Reagan Building and International Trade Center located at 1300 Pennsylvania Avenue N.W. in Washington, D.C. Please note that space is limited for in-person attendance and early registration is encouraged. You can also attend the meeting by livestream.
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Deadline to register: February 16, 2024
More about IMDRF
Established in October 2011, IMDRF is a voluntary, global group of medical device regulators who work together to advance international medical device regulatory harmonization and convergence in the field of medical devices. More information on IMDRF is available at www.imdrf.org.
Questions?
If you have any questions about IMDRF or this year’s public meeting, please contact the Secretariat at IMDRF2024@fda.hhs.gov.
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