Online Training 2015 - Corrective and Preventive Action utilizing the theory of Lean Documents. - By Compliance Global Inc

Overview:
The Theory of Lean Documents is the product of applying lean principles to the creation, design, process, and management of controlled documents typically found in regulated industries. Just as lean principles challenge traditional process concepts and "push" systems, many traditional document practices are artefacts of a flawed approach. Document management systems present a fresh departure from these practices, while building upon proven principles. Lean configuration comes from the same principles, utilizing the unique power of software solutions to take over functions that had previously burdened controlled "paper" documents.
Why Should You Attend:
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 quality assurance 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 Management System Regulation, 21 CFR Part 820, and ISO 13485 as it applies to Corrective and Preventive Action
?Alignment of the Six Sigma DMAIC method 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
Learning Objectives:
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 quality assurance 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.
Who Will Benefit:
Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
?R&D Professionals
?Manufacturing Engineering
?Design Assurance
?Quality Assurance
?Operations
?Document Control
Level:
Beginner
For more detail please click on this below link:
https://www.complianceglobal.us/product/700082
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515