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