Event

Introduction to Medical Device Submissions

March 7, 2012, March 8, 2012 iCal

Location: Los Angeles, CA

Course Description:

This course covers current FDA regulatory compliance with respect to developing and marketing medical devices. A focus will be placed on relevant aspects of FDA regulations and the practical aspects of bringing a medical product to market.

The course will initially cover the general context for medical device regulations. Later, a more in-depth discussion will begin to look at each of the submission categories in detail. FDA’s regulations, guidance documents, and on-line informational resources will be highlighted and used throughout the course.

For more information, please visit: http://www.cfpie.com/showitem.aspx?productid=127&source=lsam

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