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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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October 16, 2012 |
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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.
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Organized by:
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Center for Professional Innovation & Education, Inc. |
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Invited Speakers:
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Contact info@cfpie.com for a list of course instructors
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Deadline for Abstracts:
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n/a
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Registration:
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http://www.cfpie.com/showitem.aspx?productid=127&source=hummolgen
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E-mail:
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info@cfpie.com
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