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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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January 06, 2012 |
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Center for Professional Innovation & Education (CfPIE), Dublin, Ireland
May 17 & 18, 2012
This course will be of great value to medical device professionals involved in post market surveillance. Upon completion of this course, participants will understand all the processes involved in post market surveillance, as well as the requirements of effective complaint handling programs. Attendees will be able to recognize the differences between complaints and reportable events, the parameters set for corrections, removals and recalls and differentiate between various types of post approval studies. Additionally, special attention is given to typical FDA enforcement actions.
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Organized by:
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Center for Professional Innovation & Education |
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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=092&source=hummolgen
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E-mail:
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info@cfpie.com
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