FDA new device guidance planned for 2008.

The full list of planned guidances are at the link provided. Some of proposed general guidances that may be relevant to software include:-Computer-assisted Detection Devices for Radiological Images and Data
-Electronic Copies and Electronic Submissions of Data
-Risk Management Information in Premarket Submissions
-60601-Third Edition in submissions

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IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software training course in Boise, Idaho. 3-Day course.

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