MES 2013 — CBI’s 8th Annual Forum on Manufacturing Execution Systems
Manufacturing Excellence — Implement, Deploy, Integrate and Maintain MES
Build and Deploy Effective MES Projects within a Highly Regulated Industry
CBI is proud to announce MES 2013 — The only Forum to address innovative efforts within the pharmaceutical, biotech and medical device industry. MES is necessary for process control, QA/QC, better yield, reduced reliance on paper batch records and FDA compliance. With an outstanding turnout in 2012, the 2013 forum is expected to be our best yet, uniting MES professionals to discuss how to develop, deploy and maintain an effective automation and manufacturing execution system within a regulated environment.
Key topics include:
MES integration with other shop floor systems
FDA expectations and regulatory requirements
MES in emerging countries
Multiple deployment strategies
Implementation case studies
Aligning R&D with MES
Discrete and process manufacturing
