Using Risk Management Tools with the Risk Traceability Summary

Instructor: Edwin L Bills
Product ID: 701499
Training Level: Advanced
  • Duration: 85 Min

recorded version

1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Feb-2010

Training CD / USB Drive

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(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

This Risk Management Webinar/training will discuss how to use the 5 different tools which should be used in risk management process as per ISO 14971. It also emphasize on the documentation of results of the usage of tools.

Why Should You Attend:

An effective Risk Management process requires the use of more than one tool to identify hazards and estimate risks. The use of a single tool does not produce a complete risk analysis nor does it meet the requirements of the risk management standard and FDA regulations. The standard requires identification of hazards in the device normal and fault condition. Most tools identify fault condition hazards, but omit the normal condition hazard. ISO 14971 identifies five different tools, but many companies only use one. In addition, new requirements for product use were identified by FDA in guidance on human factors and risk management in 1999, and further explored in standards on usability and human factors. The documents provide additional tools for identification of normal and fault condition hazards.

This presentation will explore effective use of the various tools for identifying hazards, hazardous situations, and estimating risk as part of the risk management process. We will identify correct use of the tools and how the results of their use should be documented in such a way that it meets the requirements of a Risk Management File in ISO 14971. We will identify strengths and weaknesses of the various tools, as well as the proper use of each tool.

Areas Covered in the seminar:

  • Regulatory and risk standards requirements and guidance.
  • Identifying risk management tools and their use.
  • How some tools are commonly misused in risk management.
  • Explaining the strengths and weaknesses of the various risk management tools.
  • Choosing the proper tools for risk management.
  • How usability relates to risk management.

Who will benefit:

This webinar is appropriate for all medical device risk management team members who use the various tools to conduct risk analysis and risk assessment, both during product and manufacturing process design and in later phases when products and their manufacturing processes are changed. It is also appropriate for supplier quality engineers who work with suppliers in developing their manufacturing processes.
  • Design Engineers
  • Quality Engineers
  • Risk Managers
  • Process designers
  • Process Validation Engineers
  • Supplier Quality Engineers

Instructor Profile:
Edwin L. Bills, During his 20 year career in medical devices, Mr. Bills has held a number of quality and regulatory affairs positions. Mr. Bills is ASQ Certified as Quality Engineer, Quality Auditor, and as Manager of Quality/ Organizational Improvement. He also holds a certificate as Regulatory Affairs Certified through the Regulatory Affairs Professionals Society, and a BS and Masters degree from the University of Cincinnati. Recently, Mr. Bills served as US Industry Co-chair of the Association for Advancement of Medical Instrumentation committee, QM/WG04, on application of risk management to medical devices and is a current member of this group.

Mr. Bills has presented at training courses for the American Association of Medical Instrumentation (AAMI) in the area of risk management and quality systems. Currently, Mr. Bills is the Principal Consultant at Bilanx Consulting LLC in the area of medical device quality, regulatory, product liability and risk management.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

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