Medical Device Manufacturers
Whether you're designing medical devices or work in the quality systems, regulations, or software/cybersecurity fields, you're making a difference to ensure that clinicians and patients are utilizing health technology that is both safe and effective.
Upcoming Courses
Quality Systems
Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485 (Nov24)
Nov 18 to Nov 22, 2024
Software/Cyber
Medical Device Software Validation (Feb25)
Feb 10 to Feb 12, 2025
Quality Systems
Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485 (April25)
Apr 14 to Apr 18, 2025
Software/Cyber
Production & Quality System Software (April25)
Apr 23 to Apr 24, 2025
Software/Cyber
Medical Device Software Validation (May25)
May 20 to May 22, 2025
Quality Systems
Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485 (Aug25)
Aug 18 to Aug 22, 2025
Stay Connected
AAMI Blog
User Experience and design thinking can be applied in every stage of the product design, development, marketing, and postmarket surveillance, writes a clinical engineer on the AAMIBlog.
Connect and Network
Be a part of the conversation with online access to AAMI Connect, a members-only discussion platform covering hundreds of topics, and network with the global health technology community at any one of AAMI’s conferences and events.