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Medical Device - Engineering Change Control Webinar  

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Development Engineers, Production Management, Engineering management, Regulatory personnel, Quality Control personnel, Quality assurance personnel, Research and Development, Software Maintenance, Process Design and Development

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Seminar Summary:

This webinar can help you control your engineering change process, reduce your change order cycle times and eliminate ambiguity when communicating product changes to your extended supply chain. (see full course description)

 

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Training Course Syllabus:


Medical Device - Engineering Change Control

Companies need to be able to adapt quickly in today´s constantly changing environment, and often that means making changes to their products. Engineers make modifications during development and production with the intent of adding functionality, improving manufacturing performance or addressing the availability of a particular part. To make sure proposed changes are appropriately reviewed, a solid process is critical especially if members of your product team are scattered across multiple locations (for instance, design engineers in Boston, the manufacturing team in St. Louis and component manufacturers all over the world). At the heart of a solid change process is the engineering change order.

Objectives of the Presentation

The stages of the engineering change process
Issue identification & scoping
Engineering change request creation
Engineering change request review
Engineering change order Creation
Engineering change order review
Engineering change notification/notice (ECN)
Change implementation
Engineering change order benefits
Pre release and post release change control
Change transfer between company and suppliers

Why Should you Attend

FDA and ISO call for change control but do not provide any further guidance as to how to create a compliant system. The situation gets complicated when a company has suppliers or contract manufacturers and changes and approvals must pass from one to the other. This webinar will describe a system, based on the regulations and years of practical experience that will allow for efficient control of the change process. It will be compliant but not cumbersome or overly time consuming.

The difference between pre release and post release change control will be explained. Methods to control the transfer and approval of changes between the company and its suppliers or contract manufacturers will be explained. Change control forms will be provided and described in detail.

Areas Covered

What is an engineering change order?
Where does an ECO fit in the engineering change management process?
Change control procedure
Pre release and post release change control
Change transfer between company and suppliers
Forms and SOP´s

Who will Benefit

Development Engineers, Production Management, Engineering management, Regulatory personnel, Quality Control personnel, Quality assurance personnel, Research and Development, Software Maintenance, Process Design and Development

Topic Background

An engineering change order (ECO) is a documentation packet that outlines the proposed change, lists the product or part(s) that would be affected and requests review and approval from the individuals who would be impacted or charged with implementing the change. ECOs are used to make modifications to components, assemblies, associated documentation and other types of product information. The change process starts when someone identifies an issue that may need to be addressed with a change to the product. It ends when the agreed-upon change is implemented. ECOs are used in between to summarize the modifications, finalize the details and obtain all necessary approvals.

Seminar Summary:

This webinar can help you control your engineering change process, reduce your change order cycle times and eliminate ambiguity when communicating product changes to your extended supply chain. (see full course description)

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