AAMI’s International Conference on Medical Device Standards and Regulation (ISC) has been the must attend event for leaders involved in the development and adoption of medical devices standards. Building on that success and recognizing the incredible opportunities and challenges that lie ahead, AAMI is pleased to announce a new and expanded format for this critical industry event. The AAMI International Conference on Medical Device Standards, affectionately known as ISC among attendees, will now become AAMI neXus.
ISC has traditionally been limited to those with direct involvement in the development or adoption of medical device standards and attendance has been limited to less than 300. Now, we’re expanding to welcome twice as many attendees and adding a focus on the application of medical device standards. This will round out the event to cover the three pillars of standards success: Development, Adoption, and Application.
Who Should Attend?
If you are actively involved or want to be involved in the development and adoption of medical device standards as a manufacturer, regulator, or healthcare professional, AAMI nexus will offer you unparalleled engagement opportunities and information. At AAMI neXus you will hear directly from and interact with the industry and regulatory leaders who are driving both Development and Adoption of existing standards, as well as planning future standards works. This is your chance to get involved and help shape the future of medical device standards!
In addition, if you rely on medical devices standards in your work, AAMI neXus is for you! AAMI is the leading provider of medical device quality systems training in the world, and we’re leveraging that expertise to create the Application track at AAMI neXus. From updates to hands-on workshops to office hours with AAMI Faculty, AAMI neXus will be the place to be to ensure you stay up-to-date on all the latest developments in medical device standards. You’ll also have the chance to meet and network with your peers and colleagues from industry and global regulatory bodies in a setting that’s focused exclusively on our medical device industry