Corrective and Preventive Action webinar at fremont 2017

OVERVIEW:

Medical Device managers, engineers, QA personnel, as well as lean program leaders. Do you find yourself constantly struggling to create, manage, and maintain all of the information found in Corrective and Preventive Actions (CAPA)which is often redundant, repetitive, and chained together in a cumbersome way?

 

Do you find that your design and manufacturing resources are spending way too much time on documenting the CAPA process and not enough time on actually correcting and preventing systemic issues? This webinar presents a fresh new approach based upon solid principles and proven practices - as well as an alternative that avoids many of the pitfalls of traditional ways of preparing these documents.

Areas Covered in the Session:

• Brief introduction to Lean Documents and Lean Configuration
• Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to design control documents
• Alignment of the Six Sigma DMAIC approach to CAPA
• Applying lean principles to documenting and tracking non-conformances
• Applying lean principles to investigating and resolving non-conformances
• Applying lean principles to instituting corrective and preventive actions

Who Will Benefit:

• Managers, Supervisors, Directors, and Vice-Presidents
• R&D
• Manufacturing Engineering
• Design Assurance
• Quality Assurance
• Operations
• Document Control

IMPORTANT DATES:

Webinar Date: Wednesday, January 4, 2017 | 10:00 AM PST | 01:00 PM EST

Duration: 60 Minutes

Others Details

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