|Event Date/Time: May 09, 2012||End Date/Time: May 10, 2012|
|Early Registration Date: Apr 06, 2012|
13 industry presentations delivered by regulatory experts from leading pharmaceutical companies
9+ hours of networking with senior regulatory affairs professionals
Practical advice on how to determine implementation dates, use annual reporting and manage a variation in eCTD.
Industry case studies examining experiences of the 1234/2008 guideline including overcoming the hurdles of grouping variations and worksharing
Learn how to use the article 5 procedure and handle variations via the MRP procedures
Expert advice on how to prepare for the implementation of article 57 and XEVMPD