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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency

 
  November 29, 2012  
     
 
ComplianceOnline, Grand Hyatt San Francisco 345 Stockton Street, San Francisco, CA 94108
2013-01-24


Course Description:

The medical device risk management (ISO 14971) course will be given using an interactive workshop format taking attendees through all of the risk management activities required by ISO 14971.  Exercises are aimed at demonstrating efficient and effective use of risk management, including best practices in applying the standard.  Emphasis is placed on practical solutions to practical problems.

Learning Objectives:

  • To educate attendees on the reasons for risk management and the central role it plays in the product life cycle.
  • To demonstrate the requirements of ISO 14971 and how to meet them.
  • To provide practical application experience in the process and tools of risk management.
  • To establish the necessary skills to identify, analyze, and control risks.

 

 
 
Organized by: ComplianceOnline
Invited Speakers:

Instructor:

Harvey Rudolph
Risk Management Consultant, HRRM LLC

Dr. Harvey Rudolph is an independent risk management consultant specializing in process development and training in risk management. He has been a member of the Joint Working Group on Risk Management since it began in 1995 and is a primary author of ISO 14971. Currently he co-chairs the US Technical Advisory Group for that standard and is working on the new ISO risk management guidance document.

 

 
Deadline for Abstracts: 2013-01-23
 
Registration: http://www.complianceonline.com/ecommerce/control/seminar?product_id=80076SEM&?channel=hummolgen
E-mail: referral@complianceonline.com
 
   
 
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