ComplianceOnline

Integrating Risk Management into the CAPA System

Instructor: Edwin L Bills
Product ID: 700525
Training Level: Basic
  • Duration: 90 Min

recorded version

$229.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jul-2014

Training CD

$299.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar will explain what FDA expects in incorporating risk in the CAPA process, what strategies can be used to assign resources to CAPA activities, and how to manage multi-level CAPA processes so that they will not run afoul of the FDA during inspections

Why Should You Attend:

CAPA findings in FDA inspections continue to be among the highest observations cited by investigators. This fact means that manufacturers should focus efforts on improving CAPA systems which are important to correcting and improving quality systems. FDA has provided information explaining that risk is an important consideration in the CAPA process. They do not however, provide any guidance on how risk is included in this important process. Additionally, more information is flowing out of FDA indicating that risk is becoming an additional focus of the agency, such as in the recent report on risk communication.

This webinar will examine regulatory and standards requirements of CAPA processes as they relate to risk management. It will discuss multi-level CAPA processes, and assigning resources to CAPA investigations, and corrective and preventive actions. This webinar will also examine the requirements for CAPA effectiveness checks, as well as integrating risk management into recall decisions and health hazard evaluations.

Areas Covered in the Webinar:

  • How to establish a multi-level CAPA process that meets requirements
  • Using risk management to assign CAPA resources and priorities
  • Updating risk management files with information from CAPA process
  • Risk management and CAPA effectiveness checks
  • How risk management integrates with recall decisions and health hazard evaluations
  • Risk management and supplier corrective actions

Who Will Benefit:

This webinar is appropriate for all personnel associated with the CAPA process. The program is not limited to those with direct operation of CAPA, but also includes all personnel that may be affected by CAPA activities.

  • Quality Auditors
  • Quality Engineers
  • CAPA Managers
  • Supplier Quality Personnel
  • Risk Managers
  • Process Engineering Personnel

Instructor Profile:

Edwin L. Bills, is the Principal Consultant at ELB Consulting in the area of medical device quality, regulatory, product liability and risk management. During his 26 year career in medical devices, Mr. Bills has held a number of quality and regulatory affairs positions. Mr. Bills is ASQ Certified as Quality Engineer, Quality Auditor, and as Manager of Quality/ Organizational Improvement. He also holds a certificate as Regulatory Affairs Certified through the Regulatory Affairs Professionals Society, and a BS and Master’s degree from the University of Cincinnati. Recently, Mr. Bills served as US Industry Co-chair of the Association for Advancement of Medical Instrumentation committee, QM/WG04, on application of risk management to medical devices and is a current member of the international technical committee. He has presented at training courses for the American Association of Medical Instrumentation (AAMI) in the area of risk management and quality systems.

Follow us :
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Computer System Validation - Reduce Costs and Avoid 483s

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.

If you have any concern about the content of the webinar and not satisfied 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 customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed
    Loading