Integrating a Quality Management System and Risk Management for Medical Devices 2011
конференции > Education, Training конференции > Integrating a Quality Management System and Risk Management for Medical Devices
February 24 - 25, 2011
Irvine CA , США
This 2 days ComplianceOnline seminar covers the essential elements of a medical device quality management system involved in creating an effective Risk Management system. Using ISO 13485 as a model, the seminar covers the QMS essentials that have the most direct impact on Risk Management. These QMS activities include product planning, design and development, supplier management, process validation, customer complaints, internal quality audits, corrective action, preventive action, and post-market surveillance. In addition, the seminar clarifies the requirements for verification and validation. The material compares and contrasts ISO 13485 and FDA QSR requirements.
Место проведения
Location: Hilton Irvine/Orange County Airport
Обратная связь
18800 MacArthur Blvd Irvine , USA
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Integrating a Quality Management System and Risk Management for Medical Devices February 24 - 25, 2011