We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » IMDRF Targets 2015 for Completion oOf Device Software Framework
IMDRF Targets 2015 for Completion oOf Device Software Framework
International device regulators laid out their agenda for the next two years, with plans to finalize a regulatory framework for software as a medical device and guidance on international sharing of adverse event data in 2015.