Do you Know how UDI is used throughout the life of a device? Who Needs it? When do they need it? And what happens if it’s not available?
These questions and more are answered by Madris Tomes, the former FDA UDI Program manager and project manager for MAUDE (CDRH’s adverse event reporting system).
4/27/2017AIM to Host Data Capture Event at LIVE!
4/19/2017AIM NA Announces New Committee Leadership
3/14/20172017 AIM Award Winners Announced
5/2/2017 » 5/3/2017The 3rd Annual Asia-Pacific Spectrum Management Conference
5/3/2017 » 5/4/2017UK e-Health Week
5/3/2017 » 5/4/2017NPMA Spring Education Seminar