Get Tough on Corrective Actions

Instructor: Larry Whittington
Product ID: 701822
  • Duration: 60 Min
This CAPA audit training will discuss how auditors need to be tough in evaluating corrective action so that it will help in removing nonconformity in the future rather than only fixing the problem and not removing the cause.

recorded version

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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jan-2011

Training CD / USB Drive

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Read Frequently Asked Questions

Why Should You Attend:

Do you seem to be reporting some of the same nonconformities from audit to audit? Isn’t that frustrating? Why isn’t the auditee fixing the problems? It may be partly your fault. Accepting weak corrective actions will lead to repeat nonconformities. Auditors must get tough when evaluating corrective actions. If the action only fixes the problem and doesn’t remove the cause, don’t accept it. If you accept a weak solution, you’ll end up writing the same nonconformity in the future.

Why are organizations having a hard time taking effective corrective action? It may be they don’t understand how to perform root cause analysis. Or, it might be they simply view a request for corrective action as a distraction to be quickly dismissed so they can get back to work.

A common mistake is for the auditee is to say the root cause was “human error”. As a result, they attempt to correct the guilty person’s behavior instead of eliminating the real root cause. Unfortunately, auditors often compound the issue by attempting to conduct the follow-up audit too soon.

This session reviews the differences between containment, correction, corrective action, and preventive action. Common issues are identified and auditors are told to get tough on corrective actions. They must reject weak responses. If not, they’ll repeatedly report the same or closely related nonconformity.

Areas Covered in the Webinar:

  • Repeated Nonconformities.
  • Cause Really Human Error?
  • The Auditor Role.
  • Corrective Action.
  • Corrective Action Request.
  • Corrective Action Process.
  • Appropriate Action.
  • Correction vs. Corrective Action.
  • Correction Example.
  • Requirements for Correction.
  • Related Terms.
  • Correction Types.
  • Corrective Action vs. Preventive Action.
  • Audit Example.
  • Problem Solving.
  • Conclusion.

Who Will Benefit

All industries conducting internal audits of their ISO 9001-based quality management systems will benefit from this session

  • Internal audit program manager
  • Audit Program Managers
  • Internal auditors

Instructor Profile:

Larry Whittington, is president of Whittington & Associates, training, consulting, and auditing company founded in 1993 and located in Woodstock, Georgia. He is an RABQSA certified Lead Auditor and IRCA Principal Auditor, as well as, ASQ certified Quality Auditor and ASQ certified Software Quality Engineer.

Larry has developed requirements, implementation, documentation, and auditing courses used by multiple training firms, and has taught hundreds of classes to thousands of students. His free monthly e-Newsletter on quality and auditing topics has been published for more than ten years and is read by thousands of subscribers.

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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.

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