Essentials of ERM and Assessing its Effectiveness Using ISO 31000

June
 4 - 5 
v
EMBASSY SUITES CHICAGO - DOWNTOWN/LAKEFRONT, 511 N Columbus Dr, Chicago, IL 60611, USA
View Map

Course Description:

If an internal audit is to assess the effectiveness of the organization's risk management program, every member of the audit team has to understand the underlying principles.

This two-day course on ERM will introduce internal auditors to the principles and practices of risk management. It is a course for all types of organizations, whether public or private, and in all sectors and industries.

This course will focus on the ISO 31000:2009 global risk management standard. It will also cover some of the principles behind the alternative COSO Enterprise Risk Management - Integrated Framework. This will enable auditors from organizations who have adopted COSO rather than ISO to assess the effectiveness of their risk management program.

This ERM course will:

  • Discuss each of the ISO 31000:2009 principles and how they may be achieved.
  • Review the essential elements of a risk management program: the framework and process.
  • Discuss the issue of risk appetite (a COSO term) and risk criteria (the ISO term): what is needed for this to be effective for an organization.
  • Discuss several tools for assessing the maturity of risk management, with increasing levels of detailed guidance.
  • Address the issue of how internal audit can contribute – whether through consulting or assurance engagements.

The course will spend quality time considering how the assessment of risk management effectiveness should be performed, both its design and operating effectiveness. Finally, attendees will review and discuss how the results of this assessment should be communicated to stakeholders.

Norman Marks, an Honorary Fellow of the Institute of Risk Management, will share his view that our perception and practice of risk management must undergo a radical shift if it is to be effective. He will share his thoughts on:

  • Why are risk management programs failing? What are they missing?
  • How can risk management contribute to organizations taking the right risks?

Learning Objectives:

Participants will gain a solid understanding of the principles behind mature and effective risk management programs, together with the concepts and approaches necessary for an assessment of whether the program meets the needs of the organization.

Who will Benefit:

The course will cover essential material for any internal audit executive and is also relevant for auditors charged with understanding and assessing their organization’s risk management program. It will also be valuable for those individuals who are building their skills so they can move into an internal audit leadership role. The following job titles/ positions will benefit from attending:

  • Chief Audit Executives
  • Internal Audit Directors and Managers
  • Internal Audit Seniors charged with auditing risk management
  • Chief Risk Officers
  • Heads of Market, Credit and Operational Risk
  • Leaders within the Risk Office
  • Board Members, especially Risk and Audit Committee Chairs and Members
  • Chief Compliance Officers
  • Bank Regulators and Examiners
  • Risk Management Consultants
  • Internal Audit Consultants

 

For Registration -  http://www.complianceonline.com/iso-31000-coso-enterprise-risk-management-erm-process-seminar-training-80204SEM-prdsm?channel=pickevent


Note: Use coupon code 232082 and get 10% off on registration.

Join the conversation

Upcoming events

The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals

l28 May 15 | 8:30

Course Description: All facilities manufacturing pharmaceuticals, biologics,...

Q

Elements of Current Good Manufacturing Practices

l28 May 15 | 8:30

Course Description: In this two day workshop conference you will learn the...

Q

The A to Z of Trade Compliance for a U.S. Entity

l28 May 15 | 8:30

Course Description: Trade Compliance plays a prominent role in international...

Q

Understanding the Statistical Considerations for Quantitative ICH Guidelines

l28 May 15 | 8:30

Course Description: This course is designed to introduce to individuals the...

Q

Risk Based Internal Auditing (RBIA): 2-day Comprehensive Training Workshop

l1 Jun 15 | 8:30

Course Description: Risk Based Internal Auditing (RBIA) is defined by the...

Q

Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half-day In-person Seminar

l2 Jun 15 | 8:30

Course Description: FDA inspection and oversight of quality control (QC)...

Q

Operations Risk Management and Mitigation - from Assessment to Implementation

l4 Jun 15 | 8:30

Aims Recently, a series of headline-grabbing operational risk incidents at...

Q

Human Resources and Employment Law Essentials: 2-Day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Is your company at risk for non-compliance? Is your...

Q

Managing an Effective AML Compliance Program: 2-day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Are the financial transactions within your organization...

Q

Essentials Of USP Microbiology - Reading Between the Lines of the USP General

l8 Jun 15 | 8:30

Course Description: The objective of this two day "Essentials of USP...

Q

FDA's Medical Device Software Regulation Strategy: 2-Day In-Person Seminar by Ex-FDA Official

l9 Jun 15 | 8:30

Course Description: The growth of the medical software industry outpaces the...

Q

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

l11 Jun 15 | 8:30

Course Description: Raw material requirements in a cGMP environment are often...

Q

Post-Market Compliance for Medical Devices and Evolving Reporting Requirements

l11 Jun 15 | 8:30

Course Description: This interactive one and a half day course led by Ms. Rita...

Q

Auditing the Human Resource Function & Human Resource Metrics: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: This seminar will cover auditing human resources practices...

Q

FDA's New Import Program Concerning International Consequences: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: Importing products regulated by the FDA has become more...

Q

Internal Control Best Practices for your Procure to Pay (P2P) Process

l11 Jun 15 | 8:30

Course Description: This two day seminar will focus on internal controls...

Q

Detecting and Preventing Internal and External Fraud: 2-day In-person Seminar

l18 Jun 15 | 8:30

Course Description: Organizations of all kinds and sizes are increasingly...

Q

SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

l18 Jun 15 | 8:30

Course Description: Formal written Standard Operating Procedures (SOPs) are...

Q

Building a Vendor Qualification Program for FDA Regulated Industries

l18 Jun 15 | 8:30

Course Description: If you are looking for the answer to the following...

Q

Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: A growing public demand for supplements has resulted in a...

Q

Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and...

Q

21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and industry...

Q

Supplier Management for Medical Device Manufacturers

l25 Jun 15 | 8:30

Course Description: Supplier selection and management is one of the critical...

Q

Import Procedures and Documentation

l25 Jun 15 | 8:30

Course Description: This 2-day seminar is designed to assist companies that...

Q

Project Management in Human Resources: 2-Day In-Person Seminar

l25 Jun 15 | 8:30

Course Description: Naturally, getting a project to deliver on time, within...

Q

The European Clinical Trial Directive…Plus…European Filings and Registration Procedures

l25 Jun 15 | 8:30

Course Description: This interactive two day seminar will cover the various...

Q

Compliance Processes for Life Science Products in Brazil, Russia, India, China markets

l9 Jul 15 | 8:30

Course Description: This seminar will help you understand the regulatory,...

Q

Technical and Regulatory Writing for FDA Regulated Industries

l9 Jul 15 | 8:30

Course Description: Regulatory professionals have to write highly technical...

Q

OCEG approved GRC (Governance, Risk and Compliance) Professional Seminar

l15 Jul 15 | 8:30

Course Description: This GRC Professional Seminar will teach you how to...

Q

Anti-Corruption Compliance - Understanding the OECD Anti-Bribery Convention

l26 Aug 15 | 8:30

Course Description: Bribery can often damage your business and your...

Q

Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar

l8 Oct 15 | 8:30

Course Description: This two day course will prepare firms for a quick,...

Q

Regulatory Crisis Management: Best Practices for Dealing with the Common Crisis Events

l12 Nov 15 | 8:30

Course Description: Unlike risk management, which involves managing potential...

Q