The Center for Professional Innovation & Education has designed this two-day course 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.
This program will provide a broad introduction to the subject of risk management for more experienced personnel, including middle and upper management. It will allow participants to update and broaden their knowledge of US and International Risk Management requirements. It explores both the positive and negative aspects of risk and aims to improve knowledge and practical skills in the identification assessment and control of business risk.
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 will be placed on the effective use of resources in a production and quality system environment by developing strategies based on risk.
The first day will cover the general context for risk management, required procedures and the discussion of the general ISO 14971, FDA, and GHTF requirements of risk management. The second day will discuss and apply several risk management techniques which will be covered as they relate to product and production processes.
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About The Center for Professional Innovation & Education (CfPIE)
The Center for Professional Innovation & Education is the global leader in accredited pharmaceutical training including courses on Biotech, Biopharmaceutical, Medical Device and Skin/Cosmetic product topics. With over 270 public courses and customized client-site training programs offered annually, CfPIE has a convenient option for personnel looking for both professional advancement and technical/regulatory training.