Introduction to Root Cause Investigation for CAPA

  • Vanessa Lopez
  • 10, December 2019 Tuesday
  • 10:00 AM PST | 01:00 PM EST (60 Min)

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.

Live Online Training
December 10, Tuesday 10:00 AM PST | 01:00 PM EST (60 Min)

$229.00
One Dial-in One Attendee
$599.00
Group-Max. 10 Attendees/Location
(For multiple locations contact Customer Care)

Recorded Version Only

(PPT + Recorded Streaming Link)

$299.00
1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section 48 hrs after completion of Live training

CD or USB Drive Only

(PPT + Recorded Training File)

$399.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days after completion of Live training
Customer Care

Fax: +1-650-362-2367

Email: customercare@fdatrainingalert.com

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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

Ms. Lopez 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.

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. FDATrainingAlert 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@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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