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

Speaker

Instructor: Jose Mora
Product ID: 701653

Location
  • Duration: 90 Min
In this 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.
RECORDED TRAINING
Last Recorded Date: Mar-2022

 

$299.00
1 Person Unlimited viewing for 6 month info Recorded Link and Ref. material will be available in My CO Section
(For multiple locations contact Customer Care)

$399.00
Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
(For multiple locations contact Customer Care)

 

 

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Fax: +1-650-362-2367

Email: [email protected]

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Why Should You Attend:

Controlled documents are the result of a business process, just as a manufacturing process generates a product. A document cannot move ahead if it is waiting for information or if its use is restricted by other documents, just as a product cannot move forward if it is waiting for component parts. Despite the fact that many life science businesses push for lean manufacturing, lean laboratories, and lean operations, they have cumbersome controlled documents and systems that add to operating costs and make it impossible to implement process innovations on a timely basis.

This webinar covers critical topics for integrating lean principles while staying in control and adhering to regulations. It will teach you how to use lean manufacturing principles, the theory of constraints, the DHF, DMR, and DHR, as well as how to design a lean DHF, DMR, and DHR.

Areas Covered in the 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.

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
Instructor Profile:
Jose Mora

Jose Mora
Principal Consultant, Atzari Enterprises

Jose 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.

Jose led the launch of manufacturing at a start-up urology products company as Director of Manufacturing for UroSurge, Inc. at the University of Iowa’s business incubator park in Coralville, IA, creating a world-class medical device manufacturing operation, with JIT, kanban systems, visual workplace and lean manufacturing practices.

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Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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