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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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January 06, 2006 |
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SPI USA, Inc., Portsmouth, NH
April 6-7, 2006
This seminar covers the key fundamentals for medical device companies to be granted approval from the US FDA to market their products.
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Organized by:
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SPI USA, Inc. |
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Invited Speakers:
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The course is taught by Dr. Semih Oktay, former scientific reviewer at the U.S. Food and Drug Administration (FDA) and President and founder of CardioMed Device Consultants, LLC. and Dr. Antonio Moreira, Executive Vice President of SPI USA, Inc.
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Deadline for Abstracts:
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n/a
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Registration:
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Please visit website for details!
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E-mail:
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nhawkins@usaspi.com
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