home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Courses and Workshops  
 

Training Course on CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3

 
  July 12, 2011  
     
 
Radisson Blu Hotel , Abu Dhabi, UAE
Nov 27 2011 7:00AM - Nov 29 2011 3:00PM


High Quality of a registration dossier facilities the registration procedure - Essential for Generics!

This Module provides a comprehensive description on the Common Technical Dossier structure - completely updated to reflect the latest changes in pharmaceutical regulatory affairs. The course is focusing on the specific regional EU requirements for Module 1 including discussion of the relevant legislation.
The requirements for the Quality documentation (Module 2.3 & 3) will be presented in detail, taking into account the recent ICH-Q guidelines.
The course is for new developments, but is also very much attractive for Generics. In addition, this training course addresses Quality by Design aspects and issues.

 

Event Code:
11533

 

 
 
Organized by: DIA Europe
Invited Speakers: See website for speaker information
 
Deadline for Abstracts: Call contact
 
Registration: DIA Europe

ELISABETHENANLAGE 25, POSTFACH

4002 BASEL

SWITZERLAND

 

TEL.: +41 61 225 51 51

FAX:  +41 61 225 51 52

E-mail: diaeurope@diahome.org
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.