Standards, regulations and software development best practices in medical device software are constantly evolving, with more aspects to consider than ever before and teams becoming progressively more agile.
Being truly agile in such a regulated environment is a challenge, and manufacturers constantly seek to improve the quality, usability and software lifecycle of their device development.
SDMD is the only truly international forum dedicated to medical device software development & compliance, and as of 2013 is now a complete one-stop-shop for all RA/QA and Software Engineers involved in medical device development.
From: January 27, 2014 09:00
To: January 30, 2014 17:00
Hotel Excelsior, Schuetzenstrabe 11, 80335, Munchen, Germany