Event : Managing the Software Development Life Cycle to Produce Regulatory Documentation (for Medical Devices) http://www.rsc.org/events/detail/9752/Managing%20the%20Software%20Development%20Life%20Cycle%20to%20Produce%20Regulatory%20Documentation%20(for%20Medical%20Devices) This is a feed for event : Managing the Software Development Life Cycle to Produce Regulatory Documentation (for Medical Devices) Thu, 11 Sep 2014 13:13:13 +0100 9752 9752 http://www.rsc.org/events/detail/9752/Managing%20the%20Software%20Development%20Life%20Cycle%20to%20Produce%20Regulatory%20Documentation%20(for%20Medical%20Devices) Managing the Software Development Life Cycle to Produce Regulatory Documentation (for Medical Devices) Event dates: 22 October 2013<br/>Event summary: This webinar will discuss regulatory requirements for the medical device software development process and how the documentation needed for MDD technical files and for FDA submission can be developed<br/>Event Venue: Online Event, Palo Alto, 94303, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00