10.00 Introduction
10.10 Operational improvement in a high volume solid laboratory dose QC
11.10 Finite capacity scheduling in the QC laboratory
11.50 Six-Sigma impact in the laboratory environment in 3M
12.30 Lunch
13.30 Rapid microbiological methods
14.10 Overview of medium throughput automation
14.50 Central data repositories for improved data analysis and decision making
15.30 Electronic note books and integration to LIMS
Ray Munden, Chairman, Joint Pharmaceutical Analysis Group
Clair Weavers-Hamilton, Sanofi-AventisChris Dale, Business Transition Technologies
Kanny Claire, 3M Healthcare
Jon Faulkes, AstraZeneca
John Trigg, Phase Four Informatics
Two more to be confirmed.
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