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Thursday, January 19, 2012 Webinar Beyond Compliance: Turn FDA Initiatives into Impetus for Higher Product Quality, Growth and Profitability
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February 16, 2012,
1:00 pm ET
Speaker:
Mark Lincoln
Vice President of Quality and Operations,
Terumo Cardiovascular Systems
Terumo is adopting a closed-loop approach to product quality – rather than focusing only on their traditional compliance-focused processes – and will be able to drive more business value from: Good quality processes, early detection and prevention of issues, the visibility to quickly find and correct root causes, and enforcement to drive consistency across all plants. The initiative has helped the company increased productivity and output while it reduced:
- Production nonconformances (NCRs) and process issues by 41%
- Workmanship complaints by 65%
- Overall complaints (CPMs) by 58%
Attend this important webcast to learn:
- Characteristics of a low-risk, high quality operation
- How to turn FDA regulations into an impetus for proactive business decisions that enable higher product quality, growth and profitability
- How Terumo's Platform approach with MES, QMS and Intelligence enables this continuous improvement
- Specific positive business results of embracing a closed-loop approach
- Recommendations for manufacturers in any industry on how to view quality from the customer perspective.
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Friday, November 13, 2009 Missed a Session in Camstar's Solution Series?
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Camstar's recent Solution Series provided an indepth view into Camstar's innovative solutions to key industry challenges and featured demonstrations of Camstar's products. If you missed any of these events, you can request access to a recorded version.
Available sessions include:
- Strategies and Solutions for Global Deployments
- Camstar Manufacturing for Advancing Product Quality
- Camstar’s Weigh and Dispense Solution
- Demonstrating Camstar’s SolarSuite™
- The Next Generation CAPA System
- Extending Nonconformance Reporting to Nonconformance Management
- Next Generation Complaint Handling for the Medical Device Industry
Request Access
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