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  LIMS  
  July 30, 2002

Others

 
     
  Barnett International, Philadelphia
Sept. 19-20, 2002


Proven Best Practices to Overcome Common Pitfalls and
Meet Regulatory Expectations

· Strategies for 21 CFR Part 11 Compliance - Moving Towards a Paperless Laboratory
· Implement LIMS Using Proven Strategies Employed in Industry
· Increase LIMS Integration and Interfacing Capabilities
· Employ Industry Best Practices for LIMS Validation
· Improve Vendor Selection and Vendor Management Processes
· Use XML to Interface LIMS and Electronic Lab Notebooks (ELN)
· Examine Cost Effective Strategies for Efficient Upgrades
 
 
Organized by: Justin Browne
Invited Speakers: Randy C. Hice
Keir Evans, Technical Team Leader, Bristol-Myers Squibb
Victor Rivera, CSQE, Computer Validation Manager, Amgen Inc.
William D. Devorick, MS, MBA, Relationship Manager, Laboratory Automation Systems, West Pharmaceutical Services
Bhanu Sharma, Manager, IS Compliance & Validation, Bayer Corporation
Joanne M. Watson, Validation Manager, Immunicon Corporation
Richard A. Agresta, Sr. Analytical Chemist, AstraZeneca Pharmaceuticals
Sam Yazdani, LIMS Administrator, Gilead Sciences
Keith Wipprecht, Director of Pharmaceutical Sales & Marketing, LabWare, Inc.
T. R. Gilmore, Senior Technical Staff Member, Developer of the 1st Commercial LIMS, Beckman Coulter Inc.
 
Deadline for Abstracts: passed
 
Registration: 215-492-9000
E-mail: lisa.zoks@parexel.com
 
  Posted by:   justin brown  
Host: 24-90-9-192.si.rr.com
   
 
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