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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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November 11, 2005 |
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SPI USA, Inc., Miami, FL
January 26-27,2006
This 2-day workshop presented by SPi USA, Inc. in collaboration with CardioMed Device Consultants, LLC. will aid you in learning and understanding such topics as: How to interact wiht the FDA; Device Classification, and Regulatory Requirements to Pre-market Approval (PMA); the FDA Inspection Process; Quality Systems Regulations and more!
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Organized by:
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SPI USA, Inc. |
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Invited Speakers:
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Former FDA Scientific Reviewer, Dr. Semih Oktay and Executive VP of SPI USA, Inc., Dr. Antonio Moreira.
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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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