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MEDICAL DEVICES 2011 - An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971 - Medical Devices webinar By ComplianceOnline
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701773?channel=ourglocal |
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Category Medical Devices,conference,event,Webinar
Deadline: January 10, 2011 | Date: January 10, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2010-12-03 18:07:28 (GMT+9)
Call For Papers - CFP
This Integrated Risk Management Approach training in ISO 14971 will discuss how to incorporate risk management as per ISO 14971 in all phases of medical device development and what all documentation to be gathered to support the decisions made as a part of risk management process.Areas Covered in the Seminar:How are risk management activities integrated throughout the development process.The roles that Hazard Analysis, FTA, FMEA, HAZOP and PFMEA play in an Integrated Risk Management Process.How to control and verify risk mitigations.How to perform a Risk Benefit Analysis on ALARP and INTOLARABLE Hazards.The importance of maintaing Risk Management documents in the Post Production era.What information to include in the Risk Management Plan and Report for better auditability.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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