ComplianceOnline

Introduction to Root Cause Investigation for CAPA

Instructor: Vanessa Lopez
Product ID: 704409
  • Duration: 60 Min

recorded version

$249.00
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

Training CD

$349.00
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 CAPA training program will provide an understanding of FDA and ISO requirements, steps in CAPA process and the challenges associated to root cause analysis. Attendees will learn the tools and quality data sources to use during root cause analysis investigation.

Why Should You Attend:

If you have reoccurring problems showing up in your quality systems, your CAPA system is not effective and you have not performed an in-depth root cause analysis to be able to detect through proper problem solving tools and quality data sources, the true root cause of your problem. Unless you can get to the true root cause of a failure, nonconformity, defect or other undesirable situation, your CAPA system will not be successful. Historically, 483s in the medical device industry related to CAPAs, are due to lack of inadequate root cause investigations, among other factors. This course focuses on the medical device industry and provides a basic understanding on:

  1. What are the FDA and ISO (13485:2016) requirements
  2. How is root cause analysis integrated into the CAPA process and risk management
  3. Challenges associated to root cause analysis
  4. Problem solving tools to use during the root cause analysis investigation
  5. Where to find objective evidence for this type of analysis

Learning Objectives:

  • Understand the difference between a correction, corrective action and preventive action
  • Learn which medical device regulation and standard, apply to CAPA
  • Learn why root cause analysis is important
  • Understand the difference between a direct cause, a contributing cause and a true root cause
  • When to use root cause analysis during the CAPA process
  • Understand the association between root cause and risk management
  • Tools and quality data sources you may use during root cause analysis

Areas Covered in the Webinar:

  • What is CAPA vs Correction
  • FDA and ISO (13485) Requirements
  • CAPA’s Criticality in Quality Systems
  • Steps in a CAPA Process
  • Quality Data Sources for CAPA
  • Risk Management as Part of CAPA
  • What is a Root Cause Analysis (RCA)/Investigation
  • Challenges Associated to RCA
  • Difference between a direct cause, a contributing cause and a true root cause
  • Six Steps in Problem Solving
  • Steps to Follow If the Root Cause is Not Clearly Known
  • Tools Used for RCA/Investigation
  • Examples of Three of These Tools and When to Use Them

Who Will Benefit:

  • CAPA Owners
  • Quality Assurance/ Quality Control Personnel
  • Regulatory Compliance Professionals
  • Document Control Personnel
  • Regulatory Affairs Professionals
  • Quality and Manufacturing Engineer
  • Supplier Quality Managers
  • Quality Auditors
Instructor Profile:
Vanessa Lopez

Vanessa Lopez
Sr Quality Regulatory Consultant, Quality and Regulatory Consulting Services

Vanessa Lopez, Sr. Principle Quality, Regulatory and Compliance Consultant, has held a wide variety of leadership roles in the Medical Device (Class: I, II, and III), Pharmaceutical (API; Finished Product) and Environmental regulated industries as well as the Consulting Services industry. She has worked for Edwards LifeSciences, Roche Diagnostics, Eli Lilly, Pall LifeSciences, among others. She possesses over 25 years of experience focused on development, implementation, driving improvements and monitoring of Quality Assurance, Quality Control, Regulatory Compliance, Regulatory Affairs, Quality Systems and Supplier Quality activities.

Ms. Lopez has in-depth knowledge, coaches on interpretation and application of US regulations, EU directives, specific country regulations (Japan, Canada, and others), national/international standards and guidance documents. She has also held positions within the CAPA, Material, Safety and Management Review Boards as well as represented Quality in Design Control phases.

Follow us :
ComplianceOnline Medical Device Summit 2017

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).

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