Comprehensive Training on European Regulatory Affairs including Different Registration Procedures and Variations: Expert Overview

http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?pr... Course

Date(s) And Time(s):
Feb 27 2011 8:00AM - Mar 1 2011 3:00PM

Location:
Radisson Blu Hotel
Golf Plaza, Yas Island
P.O. Box 93725
Abu Dhabi
United Arab Emirates

Overview:

The ‘Comprehensive Training on European Regulatory Affairs including different Registration Procedures and Variations: Expert Overview’ training course is a key course developed by DIA in Europe. This course provides a comprehensive description and discussion of the regulatory environment. The course focuses on Europe but also looks at regulations in other regions including the USA and Japan.

Your benefit:

This is a unique opportunity to learn, understand and discuss the main aspects of drug regulations in Europe directly from key European Regulators and from the large experience in the pharmaceutical industry and to acquire key recommendations for a successful implementation of your regulatory strategy and operations.

Key Topics

Drug regulations
Role of Regulatory Affairs in drug - development / approval / marketing
Efficient interactions between regulatory agencies and the pharmaceutical industry
Regulatory strategy
Key differences of international regulatory environments

Event Code:
11541

Contact Information:
DIA Europe
TEL.:+41 61 225 51 51
FAX: +41 61 225 51 52

E-MAIL: DIAEUROPE@DIAEUROPE.ORG