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European Regulatory Affairs

 
  April 18, 2006  
     
 
Drug Information Association, Renaissance Paris Hotel La Defense, 60, Jardin de Valmy, Boulevard Cirqulire Sortie 7, Paris La Defense Cedex, France
Nov 27 2006


The workshop will provide strategic advice on how to file applications for the marketing authorizations in the European Union for staff involved in International Regulatory Affairs.

Regulatory strategy which impacts on commercial, business and licensing arrangements will be of importance to those responsible for business development.

Key Topics
•European Union.
•Centralized Procedures.
•DeCentralised Procedure.
•Mutual Recognition Procedure.
•National Procedure.
•Key Issues to Consider for Business Opportunities.
•Regulatory Strategy.
•Legal Status of Products and Switching from Rx to OTC.
•Medical Devices Legislation.
•Clinical Trial Directive.

 
 
Organized by: Drug Information Association
Invited Speakers: Brenton E. James
 
Deadline for Abstracts: -
 
Registration: http://www.diahome.org/product/9224/06505.pdf
E-mail: dia@diahome.org
 
   
 
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