Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration

Brief introduction to Lean Documents and Lean Configuration. Quality System Regulation, 21 CFR Part 820, and ISO 13485 as it applies to DHF, DMR, and DHR.
 
 
José Ignacio Mora
José Ignacio Mora
 
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Tags:
* 21 Cfr Part 820
* Iso 13485

Industrys:
* Manufacturing
* Medical

Location:
* Fremont - California - US

Subject:
* Events

FREMONT, Calif. - April 2, 2014 - PRLog -- Instructor:  José Ignacio Mora (http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500192#21666)

         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 artifacts of a flawed approach. Lean documents presents 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 ccontrolled "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 DHFs, DMRs, and DHRs - 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 documentation and not enough on engineering and design? 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.

Objectives of the Presentation:
Brief introduction to Lean Documents and Lean Configuration
Quality System Regulation, 21 CFR Part 820, and ISO 13485 as it applies to DHF, DMR, and DHR
Design History Files (DHF) content, development, and management
Device Master Records (DMR) content, development, and management
Device History Record (DHR) content, development, and management
Applying lean principles to creating, developing, and managing a DHF
Applying lean principles to creating, developing, and managing a DMR
Applying lean principles to creating, developing, and managing DHRs

Who can Benefit: Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
R&D
Manufacturing Engineering
Design Assurance
Quality Assurance
Operations
Document Control

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http://www.onlinecompliancepanel.com/ecommerce/webinar/~p...


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Tags:21 Cfr Part 820, Iso 13485
Industry:Manufacturing, Medical
Location:Fremont - California - United States
Subject:Events
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Page Updated Last on: Apr 02, 2014
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