Training Brochure
Designed to facilitate and enhance the dialog among medical device professionals from both the manufacturing and regulatory environments, AAMI’s comprehensive and interactive 2½- to 4-day training programs provide a unique learning experience for quality assurance/regulatory affairs professionals; design, process, and software engineers; risk management managers; compliance officers; and standards application managers.
Participate, share, and learn with industry and regulatory representatives from around the globe.
- To download the 2012 training brochure in pdf, click here.
- To download the 2013 training brochure in pdf, click here.