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Final Product/Process Change Notification Document # : FPCN22416X Issue Date: 2 October 2018Title of Change:Qualification of mold compound G700HF in D2PAK package in ON Semiconductor Seaman Malaysia
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How to fill out final productprocess change notification
How to fill out final productprocess change notification
01
Obtain the final product/process change notification form from the appropriate department or personnel.
02
Fill out all required fields on the form, including details about the nature of the change, reasoning for the change, and any potential impact on other processes or products.
03
Attach any supporting documentation or data that may be relevant to the change notification.
04
Review the completed form for accuracy and completeness before submitting it for approval.
05
Submit the filled out final product/process change notification form to the designated approver or department for review and approval.
Who needs final productprocess change notification?
01
Manufacturing companies
02
Quality control departments
03
Product development teams
04
Regulatory compliance departments
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What is final product/process change notification?
Final product/process change notification is a formal notification required to inform regulatory authorities about any changes to the final product or process of manufacturing.
Who is required to file final product/process change notification?
The manufacturer or company responsible for the final product/process is required to file the notification.
How to fill out final product/process change notification?
The notification can typically be filled out online through a regulatory agency's portal or via email with the necessary information.
What is the purpose of final product/process change notification?
The purpose is to ensure transparency and safety in the manufacturing process by notifying regulatory authorities of any changes that could affect the final product.
What information must be reported on final product/process change notification?
Information such as the nature of the change, reason for the change, potential impact on the final product's safety and efficacy, and any supporting data must be reported.
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