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Webinar On Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration

 
  August 07, 2015  
     
 


Compliance Trainings, Online
2015-08-23


Description :

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 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.

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 must attend webinar presents a fresh new approach based upon solid principles and proven practices - as well as an alternative, applies the Theory of Lean Documents and also formulates a corresponding Theory of Lean Configuration, that avoids many of the pitfalls of traditional ways of preparing these Key Regulatory 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 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 Will Benefit:

A must for all Managers, Supervisors, Directors, and Vice-Presidents in the areas of:

R&D

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Document Control

Lean Program Leaders

 
 
Organized by: Compliance Trainings
Invited Speakers:

José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies. During that time he prepared a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.

 
Deadline for Abstracts: 2015-08-22
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1485

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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