Improving Quality, Efficiency and Compliance with Paperless Manufacturing through eDHR and eBR Systems
March 6-7, 2013
- Chicago, Illinois
Available for $495.00
Design, Deploy and Restructure MES within a Highly Regulated Industry
MES is an extremely complex system that requires vast majority of internal resources; inclusive of time, budget and staff. Within the life sciences industry, worldwide regulatory agencies continue to update guidelines specific to GMP and additional manufacturing automation oversight. In order to successfully deploy or redesign MES, companies must understand and adapt to the changing regulatory landscape.
Hear from Medical Device, Diagnostic and Biotechnology Thought Leaders on the Following Topics Being Researched:
- CFR 21 Part 11
- Integrating MES with SCADA, ERP, SAP and the Automation Layer
- Track and Trace
- Lean Manufacturing
- Single or Multiple Deploy Strategies
- Global MES
- MES Change Management
Featuring Elite Speaker Perspectives from:
- Camstar
- Roche Diagnostics
- Boston Scientific
- B.Braun Medical Inc.
- Illumina, Inc.
- Philips
- GE Healthcare
- Terumo Cardiovascular Systems
- CIBA Vision
- Advanced Bionics
- American Medical Systems
