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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260708T183020Z
UID:f5308970-953c-42c8-8674-9f8253c3e07d
DTSTART:20171016T090000Z
DTEND:20171017T170000Z
DESCRIPTION:This two-day course is designed to provide individuals with a d
 etailed understanding of the important regulatory guidelines involved in t
 he development of a new product plan within the EU. The program will also 
 cover effective strategies for correctly applying the current regulations 
 to ensure that rejections are avoided.\n\nThe course will provide the atte
 ndee with a thorough knowledge of the following topics:\n•How to develop
  a regulatory strategy\n•How to deal with pricing and reimbursement issu
 es in your development\n•How to validate your regulatory strategy (scien
 tific advice) and how to choose between centralized and national scientifi
 c advice\n•When does your product qualify as an orphan medicinal product
  and what are the advantages if it does?\n•How to deal with pediatric de
 velopment plans\n•What has to be considered for Advanced Therapy Medicin
 al Product and oncology medicinal products\n
LOCATION:The Berlin Hilton
SUMMARY:European Union Regulatory Issues - New Product Development
URL;VALUE=URI:https://www.cfpie.com/ProductDetails.aspx?ProductID=280
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