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Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions

 
  October 16, 2012  
     
 
Center for Professional Innovation & Education, Inc., Los Angeles, CA
Feb 27 & 28, 2013


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.
 
 
Organized by: Center for Professional Innovation & Education, Inc.
Invited Speakers: Contact info@cfpie.com for a list of course instructors
 
Deadline for Abstracts: n/a
 
Registration: http://www.cfpie.com/showitem.aspx?productid=127&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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