Corrective and Preventive Action Conference

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?

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

Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
http://www.compliance4all.com/
Event Link : http://www.compliance4all.com/control/w_product/~product_id=501079LIVE?channel=mailer&camp=Webinar&AdGroup=govevents_Jan_2017_SEO
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