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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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February 27, 2007 |
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SPI USA, Inc., Frankfurt, Germany
May 9-10, 2007
This 2-day seminar covers the fundamentals for Medical Device companies to be granted approval from the US FDA to market their products. It features a section on how to interact with the FDA, taught by Dr. Semih Oktay, a former FDA Scientific Reviewer. It also includes a section on combination products, their classification and strategies for determining, influencing and negotiating the best regulatory path for the product. This seminar also includes case studies and much more!
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Organized by:
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SPI USA, Inc. |
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Invited Speakers:
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Dr. Semih Oktay, former Scientific Reviewer for the US FDA
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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 and discounts.
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E-mail:
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nhawkins@usaspi.com
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