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From:
15 Jun 2010
To:
16 Jun 2010
Location:
Budapest,
Hungary
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Regulatory Affairs in Central and Eastern Europe -new date- |
Four regulatory representatives will bring you up to speed with the latest European and national regulations and offer practical advice on accessing markets of Croatia, Serbia, Poland, Romania, and Estonia. You will gain insight into the implementation of the new Variations guideline for 2010 as well as the requirements for successfully filing applications in candidate EU countries. You will learn about registration procedures for biosimilars in CEE as well as how implementation of the eCTD across CEE will impact on your submissions.
For more information click here.
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