AAMI neXus: A Global Event Advancing Medical Device Standards Development, Adoption, and Application
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Upcoming Events
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Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485 (Nov24)
November 18 to 22, 2024Register
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Design Control Requirements - Integrating the Quality System Regulation (Dec24)
December 3 to 5, 2024Register
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Human Factors for Medical Devices (Dec24)
December 10 to 12, 2024Register
Publications
AAMINEWS
HTM Professionals Build and Implement VR Training Programs, FDA Reclassifies Medical Image Analyzers, Tech World: The Potential of Wearable Health Technology Devices, and much more.
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KEEPING IT CLEAN
Using Standards and TIRs to Drive Consistent Sterile Processing Procedures
Standards and technical information reports (TIRs) from AAMI are critical resources for anyone involved in the processing and sterilization of medical devices. Learn more in the new BI&T cover story (log in to view).
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WHAT'S NEW WITH AAMI?
Keep up with everything that is happening at AAMI! Follow us on all available social media platforms!
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