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An Advanced Course on Lean Documents, Lean Configuration and Document Control

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Website http://bit.ly/2lWqoPl | Edit Freely

Category device master record compliance, document control system, document management system, documentation process, lean manufacturing, lean manufacturing principles, lean manufacturing tools, medical device manufacturers

Deadline: April 18, 2017 | Date: April 18, 2017

Venue/Country: New Hyde Park, U.S.A

Updated: 2017-03-15 18:56:58 (GMT+9)

Call For Papers - CFP

Overview:

In this Lean Documents, Lean Configuration, and Document Control training learn the different types of lean documents and the usage of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents. Pros and cons of lean vs. non-lean documents.

Why Should You Attend:

Just as a manufacturing process produces a product, controlled documents are the product of a business process. Just as in manufacturing, a product cannot move forward if it is waiting for component parts, a document cannot move forward if it is waiting for information, or if its use is constrained by other documents. Although many life science companies advocate lean manufacturing, lean laboratory, and lean operations, they have cumbersome controlled documents and systems which cause significant operating expenses, and make it difficult to introduce process improvements in a timely manner.

This webinar presents key concepts on introducing lean principles, while maintaining a state of control and regulatory compliance. It will help you understand applying lean manufacturing principles, theory of constraints, DHF, DMR, DHR and how to create a lean DHF, DMR, DHR.

Areas Covered in this Webinar:

Definition of lean documents.

Problems with traditional document approach.

Applying lean manufacturing principles.

Applying Theory of Constraints.

Design History File.

Device Master Record.

Device History Record.

Typical challenges and how to overcome them.

Examples of various types of lean documents.

Use of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents. Pros and cons of lean vs. non-lean documents.

How traditional document approach generates waste.

Clues from Theory of Constraints and Lean Manufacturing.

What a lean document approach would have.

Creating a lean Design History File.

Creating a lean Device Master Record.

Creating a lean Device History Record.

Preparing to configure an electronic document system.

Learning Objectives:

understanding applying lean manufacturing principles, theory of constraints, DHF, DMR, DHR and how to create a lean DHF, DMR, DHR

Who Will Benefit:

This webinar will provide valuable insights to design engineers, manufacturing engineers, operations managers, quality system managers, and document control managers

Project leaders implementing an electronic document system

Functional managers

QA managers

Lean Project Managers

Speaker Profile:

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.

For more detail please click on this below link:

http://bit.ly/2lWqoPl

Email: referrals@complianceglobal.us

Toll Free: +1-844-746-4244

Tel: +1-516-900-5515

Fax: +1-516-900-5510


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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