Construction of the European Drug Master File (EDMF) for Regulatory Agencies - Webinar by GlobalCompliancePanel

31 August 2010, Wilmington, DE, United States

Introduction

This webinar will provide valuable assistance and guidance to manufacturers who must prepare and submit the Drug Master File (Active Substance Master File) to European Competent Authorities. Employees who will benefit include:

* All levels of management and departmental representatives and those who desire a better understanding or a "refresh" overview of the EDMF process and expectations
* Regulatory Affairs
* Clinical Affairs
* Quality and Compliance
* Marketing & Sales
* Distributors/Authorized Representatives
* Engineering/Technical Services/Operations
* Consultants