Compliant Documentation, Regulatory Guidance and Quality Assurance for Manufacturing Excellence in the Life Sciences Industry
- Philadelphia, Pennsylvania
Build and Deploy Effective MES Projects within a Highly Regulated Industry
CBI is proud to announce the 7th Annual Forum on Manufacturing Execution Systems (MES) 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 2011, the 2012 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. Join the only event dedicated to MES within the pharmaceutical, biotech and medical device industry!
Don’t miss industry case studies and discussions on:
- MES data for QbD and PAT
- expectations and regulatory requirements
- Review by exception
- MES in emerging countries
- Multiple deployment strategies
- Cost and change management
- Discrete and process manufacturing
Interested speakers are encouraged to submit abstracts and ideas to Erica Caron at erica.caron@cbinet.comor 339.298.2109.
