European Regulatory Affairs

Date(s) And Time(s):
Aug 9 2010 12:45PM - Aug 10 2010 4:00PM

Location:
Drug Information Association, Inc.
800 Enterprise Rd Ste 200,
Horsham, PA 19044-3509

Interest Area(s):
Clinical Research, Project Management, Regulatory Affairs

Overview:

Best-Value Course on Registration Procedures in the European Union

Learn the practical side of the approval system in the European Union and how to apply the centralized mutual recognition and national registration procedures to a variety of products.

WHAT YOU WILL LEARN

· Centralized, mutual recognition, and national registration procedures in the EU

· Official regulatory policies and other issues pertinent to successful Eu regulatory strategy

· EU regulatory strategy pertinient to commercial, business, and licensing arrangements

· Trademarks and patents

· Medical devices

· Clinical trial directive

· Legal status and switching

Event Code:
10441

Contact Information:

For detailed program information including faculty and topics, please contact:
Susan Mazak
Tel. +1-215-442-6183
Email Susan.Mazak@diahome.org

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