Course offering number:0907-709
Course ID:
2319
Proven Methods to Root Cause Analysis for CAPA
Pre-recorded Course
FREE On-Demand Webinar
Who Should Attend
This FREE 60 minute webinar is intended for those in the pharmaceutical and medical device industries who need to know the basics of Corrective and Preventive Action (CAPA) investigations, especially those in the following areas:
• Regulatory Affairs
• Quality Assurance
• Manufacturing
• Product/Process Development
• R&D
• Maintenance
Description
This FREE 60 minute webinar presents an overview of a proven methodology used to investigate and identify the root cause(s) when there has been a shift in the performance of a product, machine, equipment, work process or system. The methodology identifies the change that has occurred so that the change can be eliminated and the performance can return to its previous level. It is ideal for investigating an increase in:
• Product or service defect levels
• Customer complaints
• Negative patient reactions with the product
• Manufacturing scrap or rework
• Equipment or process aberrations
• Any performance change where a CAPA investigation
is required
Course Outline:
• Define a technical CAPA issue Highlight effective tools
• Discuss common problem solving mistakes
• Introduction to the case study
• An overview and illustration of the
investigation methodology
• Highlight effective tools
• A resource for improving investigations
• Question and answer session
• Next Steps
Other Courses of Interest
Applied cGMPs for Pharmaceutical and Allied Industries
Developing and Maintaining an Effective Complaint System
Oct 20 2010, New Brunswick, NJ
Conducting Effective Quality Audits
Oct 25 2010, New Brunswick, NJ
Design Control and Product Validation
Oct 18 2010, New Brunswick, NJ
Documentation Management and Control
Sep 27 2010, East Brunswick, NJ
Medical Device Regulatory Compliance
Root Cause Investigation for CAPA
Nov 02 2010, New Brunswick, NJ
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