Join Us For September's Webinar - Auditing A Risk Assessment - Lessons Learned On Wednesday October 6th From 1 - 2pm EST

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Join the Audit Division for our September webinar - Auditing a Risk Assessment - Lessons Learned presented by Angelo Scangas on Wednesday, October 6th from 1 - 2pm EST.

Webinar Details
Whether you work in a complex engineering company, a manufacturing environment, a hospital, or a laboratory effective risk assessments are important in the decision-making process.

A sound approach to quality risk management utilizes the knowledge and experience of the entire team in your organization. The Team includes the people participating in the risk assessment, the people executing the mitigations as well as the internal auditors who need to evaluate the effectiveness of the process. Everyone needs to work together to assure Customer and Business satisfaction.

Auditors continue to struggle with effective and efficient audit execution of Risk Assessments. Common deficiencies include an over-reliance on checklists and inadequate understanding of the documentation, including linkage of audit procedures to the risks they are designed to address.

So, what exactly does that mean? This presentation will discuss the application of risk assessments showing the vital role an effective auditor plays in maximizing the effectiveness of the Risk Management process!


About the Presenter - Angelo Scangas
Angelo is President of Quality Support Group, Inc., an International Consulting and Training Organization. Angelo has a B.S. in Chemical Engineering, M.S. in Manufacturing Engineering and a MBA.

Angelo is a senior member of the American Society of Quality and member of the ASQ Audit Division (Webinar Chair). Angelo has more than 30 years of experience in the Medical Device, Automative, Healthcare, and Chemical Industries working in product development, manufacturing engineering, quality engineering, quality assurance, and process development/improvement. His specialty areas include strategic quality planning, risk management, supply chain management, corrective and preventative action (CAPA) programs, design and development, and validation programs.

How to Register
https://attendee.gotowebinar.com/register/6350921416510510608

After registering, you will receive a confirmation email containing information about joining the webinar.

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News Audit Division 09/14/2021 6:09pm CDT

Comments

1 Comments

This webinar has been postponed to Wednesday, October 6th.

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