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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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March 01, 2012 |
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Center for Professional Innovation & Education (CfPIE), King of Prussia, PA
July 23 & 24, 2012
This course will give participants the necessary overview of the applications and procedures used within Europe to grant marketing authorizations for medicinal products, as well as, the agencies and institutions which control the regulatory process. While special focus will be given to the European Medicines Agency (EMA) and its centralized procedure, the role of localized national health authorities and other EU bodies will be discussed in depth. The course will also cover topics relating to registration of specific groups of products such as orphan and pediatric medicines, as well as, advanced therapy and herbal product requirements.
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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=031&source=hummolgen
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E-mail:
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info@cfpie.com
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