Business Risk Mgmt ISO 31000

Instructor: Edwin L Bills
Product ID: 701606
Training Level: Advanced
  • Duration: 85 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jun-2010

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

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Read Frequently Asked Questions

This Business Risk Mgmt training will guide you on ISO 31000 general risk management standard, the process model it recommends, and how companies may use the standard, and its companion risk assessment tools document ISO/IEC 31010.

Why Should You Attend:
The International Standards Organization (ISO) has sponsored the development of a general risk management standard. The purpose is to aid organizations by providing a model for implementing risk management processes throughout their organization. Following development of this standard, ISO was requested to provide information for other processes, like financial risk, project risk, and compliance risk. The pressure on companies to improve business process risk because of failures in the financial sectors has made this standard especially important. Companies need to implement risk management processes to be compliant to regulations and also to become competitive with companies that are using these tools.

During this presentation, we will explore the ISO 31000 general risk management standard, the process model it recommends, and how companies may use the standard, and its companion risk assessment tools document ISO/IEC 31010. We will also review the various terms used in this document, and their source so that we can better understand the proper implementation of risk management processes.

Areas Covered in the Seminar:

  • The ISO 31000 risk management process model.
  • Terms and definitions in ISO 31000.
  • Requirements of ISO 31000.
  • Monitoring risk and continuous process improvement.
  • Application of ISO 31000.
  • The risk assessment tools recommended in ISO/IEC 31010.
  • Use of Risk Assessment tools in a ISO 31000 risk management process.

Who Will Benefit:

  • Business Process Owners
  • Business Finance Managers
  • Business Risk Managers
  • Regulatory Compliance Managers
  • Project Management
  • Those responsible for business risk policies

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.

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