How to Develop and Implement the Successful Internal Audit Program

Speaker

Instructor: Daniel Whelan
Product ID: 700222
Training Level: Intermediate

This Internal Audit Training will discuss the tools and techniques to design, implement and maintain the internal audit system to prevent audit system problems. The internal audit system must be successful for the business to be successful.
RECORDED TRAINING
Last Recorded Date: Oct-2006

 

$249.00
1 Person Unlimited viewing for 6 month info Recorded Link and Ref. material will be available in My CO Section
(For multiple locations contact Customer Care)

$500.00
Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
(For multiple locations contact Customer Care)

 

 

Customer Care

Fax: +1-650-362-2367

Email: [email protected]

Read Frequently Asked Questions

 

Internal auditing is the key activity to ensure that your FDA or ISO compliant quality system continues to be suitable and effective.The internal audit system must be efficient, effective and most importantly, user-friendly. However, more often than not, internal audit programs can have their own inbred set of problems that may cause delays, inefficiencies and outright failure. These problems can include:

  • Perceptions of the work force
  • Workload of the audit staff
  • System design inefficiencies
  • Lack of management support
  • Poor corrective action tracking and timely closure

Without an effective, efficient and supported internal audit system, the culture of compliance will deteriorate and the loss of registration or a warning letter becomes more of a possibility. Each of these issues have been experienced and managed to closure by the presenters.

Areas Covered in the seminar:
The presentation will also provide answers to the following questions:
  • How will we select the audit staff?
  • How many auditors and lead auditors should we train?
  • To what criteria will we train our audit staff?
  • How will we schedule our audits and auditors?
  • How many audits are appropriate for a department or a requirement?
  • How will we measure corrective and preventive action effectiveness?
  • How can internal audits be measured and integrated into business metrics?
Who Will Benefit:
Anyone involved in quality audit management and/or implementation:
  • Quality Directors & Managers
  • Quality Engineers & Auditors

Instructor Profile:
Daniel S. Whelan, Mr. Whelan has more than 30 years experience in manufacturing and quality assurance, working for leaders in their respective fields such as Polaroid, Orion Research and Pfizer Hospital Products Group.

Since 1993, Dan has consulted in the medical device industry and elsewhere as Principal Consultant at Quality Assessment Services, a quality management consulting firm based in Plymouth, Massachusetts. Global assignments include work in Central & South America, and in Europe. He has been a featured speaker and presenter at local society meetings, regional and national conferences, and New England area colleges. He has also conducted public seminars and client training in a number of subjects, including: Quality Auditing, international quality management standards ISO 13485 and ISO 9000, and the US DHHS FDA’s Good Manufacturing Practices for Medical Devices. The QA Services client list includes prominent medical device manufacturers such as SynCardia Systems, Inc; Arrow International; Boston Scientific Corp.; Ethicon Inc. and Ethicon Endosurgery; Smiths Medical; GE Sensing and Accellent Inc., among others.

Mr. Whelan was an elected officer of the American Society for Quality.

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Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
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. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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