FDA Guidance: Contents of Premarket Submissions for Software Contained in Medical Devices * Free *

Date Published:
Wed, 05/11/2005

May, 2005 CDRH guidance to industry regarding software used in medical devices and software at blood establishments.  This guidance contains sections on software documentation, risk assessment & management, software change management, software of unknown pedigree (SOUP), virus protection software, and interfaces, networking, and network infrastructure.