ISO 13485 Training
ISO 31000:2009 - Introduction to Enterprise Risk Management

E-mail this product to a friend E-mail this product to a friend


Previous  Up  Next" 

ON-DEMAND WEBINAR
Access Anytime!

Access the recorded version of this webinar anytime from any computer. Attend when it's most convenient for you. You can access the webinar as often as you like from any location for ONE FULL YEAR from the date of registration.



SUMMARY
Actions undertaken by a business enterprise have risks associated with their design, development, and implementation. Risk can be qualified and quantified. Taken from ISO 31000 Risk management – Principles and guidelines, risk is a concept that has these principle components: probability of the occurrence (along with its frequency) and the consequence of that the risk (along with how severe it might be). This two-hour on-demand webinar will provide participants with an overview of the ISO 31000:2009 standard, its integral nature within a business enterprise and a quality management system, along with its methods for assessing, analyzing and managing risk in an effective manner. ISO 31000 provides a framework of risk management activities as applied to any business enterprise. From an initial analysis through risk control and risk evaluation, the probability and frequency of harm can be assessed and analyzed and thereby managed. Much of managing risk is derived from how to frame the right questions to ask as they relate to defining the enterprise’s activities and characteristics and thus define an enterprise’s risk appetite. This webinar will provide an overview of the questions and analysis done to secure the risk appetite of the enterprise along with their potential impact on risk. The learning objective of this webinar will be to provide the attendee with an understanding of risk, its analysis and management along with a contrast of the latest revisions and changes to the standard as outlined in ISO 31000:2009.


WHY TAKE THIS COURSE?
Upon the successful completion of this course, webinar participants will understand:
  • The connections of ISO quality systems to the elements and workings of risk management from risk analysis throughout the enterprise
  • The interactions of risk management elements within a quality system including management responsibility, resource management, realization, measurement analysis and corrective/preventive actions


WHO SHOULD ATTEND THIS WEBINAR

  • Individuals responsible for and who interact with enterprise quality management systems such as ISO 9001, ISO 10006 or ISO 13485
  • Quality and regulatory professionals including: Managers, Directors, Audit team members
It is recommended that the webinar attendee is familiar with the context of process based (ISO) quality management system elements.


COURSE OUTLINE
  1. Risk Management framework, mandate and commitment
  2. Risk Management policy
  3. Risk Management accountability and organizational process
  4. Resources in managing risk
  5. Risk Management Implementation
  6. Risk Management monitoring, control and continual improvement
  7. Risk Management Process
    1. Criteria
    2. Assessment
    3. Identification
    4. Analysis
    5. Treatment
    6. Options and planning
    7. Monitoring and review
  1. The webinar attendee will be provided with an overview and discussion of the concept of risk components:
    1. probability of the occurrence of harm and how often the harm may occur and;
    2. consequences of such harm and how severe said harm may be
  2. The webinar attendee will understand enterprise stakeholder interest in risk
  3. The webinar attendee will be presented with the integral application of ISO 31000 into and as a integral part of a quality management system

HOW DOES THIS ALL WORK?

After you register for the webinar, you will receive a confirmation e-mail. It will contain a Web link to access the recorded webinar through your Web browser. You can access the recorded webinar for one full year from the date of your registration. You will need the link that will be e-mailed to you each time you wish to access the webinar.

PLEASE NOTE: The link to access the webinar will be e-mailed to you immediately after you register. If you do not receive the link, please check your spam or junk mail folder.


Price: $259.00 


Quantity:   

The CE Mark: Understanding the Medical Device Directives
The CE Mark: Understanding the Medical Device Directives
The Regulatory Compliance Almanac
The Regulatory Compliance Almanac
A Basic Approach to Root Cause Analysis
A Basic Approach to Root Cause Analysis
Auditing an ISO 9001 System
Auditing an ISO 9001 System


The CE Mark: Understanding the Medical Device Directives
The CE Mark: Understanding the Medical Device Directives
$34.95
The Regulatory Compliance Almanac
The Regulatory Compliance Almanac
$99.00