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Pharmaceutical Manufacturing Science & Quality

 
  October 27, 2005  
     
 
IBC Life Sciences, Arabella Sheraton Grand Hotel, Munich, Germany
6-8 February 2006


The innovation challenge within the pharmaceutical industry throughout Europe has led to an on-going push to improve manufacturing processes. Pharmaceutical companies are striving to be leaner so that they can strip out and drive down manufacturing costs. With a focus not only on systems and technology behind manufacturing processes, but also on compliance and supply chain considerations inherent to this topic, the manufacturing area has become a serious concern for life science organisations.

IBC’s Pharmaceutical Manufacturing Science & Quality event brings solutions to your manufacturing strategy so that you can reap the rewards of lower costs, faster time to market and uncompromised quality

 
 
Organized by: IBC Life Sciences
Invited Speakers: * Neil Wilkinson, Director Global Compliance, AstraZeneca & EFPIA, UK
* Jacques Morenas, Assistant Director, The French Health Products Safety Agency, France
* Joyce Ramsbotham, International Quality Specialist, Solvay & Chairperson of the EFPIA Manufacturing-GMP Working Group, The Netherlands
* Zena Kaufman, Senior Director, Regulatory Compliance, Pfizer, USA
* Malcolm Holmes, Director, Global Quality Assurance, GlaxoSmithKline & Member of EFPIA Manufacturing & GMP Adhoc Committee, UK
 
Deadline for Abstracts: 06/02/2006
 
Registration: Contact Charlotte Hayes at charlotte.hayes@informa.com
http://www.ibc-lifesci.com/mansci
E-mail: charlotte.hayes@informa.com
 
   
 
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