November 3&4, 2008 - Berlin, Germany

Upon completion of this course, attendees will understand how to effectively meet the requirements of risk management for medical devices, pharmaceutical and biologics products and processes. Emphasis is placed on the effective use of resources in a production and quality system environment by developing strategies based on risk. Specifically, the course is designed for quality managers, engineers, auditors, regulatory/quality compliance professionals, production managers and top management interested in learning the value of Risk Management Principals and how to enhance existing systems by better utilizing resources through the optimization of risk management techniques.
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